3-23959577-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959577
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959577
    reference: chr 3
allele count: 1
allele frequency: 8.999280057595392e-6
allele num: 111120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.172+55A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.263A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.172+55A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*8+39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.172+55A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.172+55A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.939A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.172+55A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6636T>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.172+55A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.172+55A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.172+55A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.172+55A>G
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13677
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

3-23959881-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959881
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959881
    reference: chr 3
allele count: 1384
allele frequency: 1.226841592057442e-2
allele num: 112810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6940C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-50G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-50G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.567G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-50G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-50G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-50G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-50G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-50G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1243G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-50G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-50G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-50G>A
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4623
  bin: 3.25e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 1.25e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 13908
  bin: 1.75e1
  variant carriers: 314
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 7.5e0
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.75e1
  variant carriers: 232
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12769
  bin: 2.25e1
  variant carriers: 328
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 14
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-23959887-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959887
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959887
    reference: chr 3
allele count: 1
allele frequency: 8.872327211427557e-6
allele num: 112710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.573C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-44C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1249C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6946G>A
  variant of: http://identifiers.org/hgnc/17899
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9492
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16011
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

3-23959892-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959892
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959891
    reference: chr 3
allele count: 1
allele frequency: 8.784258608573437e-6
allele num: 113840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-37delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-37delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-37delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-37delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6952delG
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1256delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-37delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-37delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-37delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-37delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-37delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.580delC
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-37delC
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: TC
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD

3-23959893-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959893
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959893
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 113458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.579C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6952G>A
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-38C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-38C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-38C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-38C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-38C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-38C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-38C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1255C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-38C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-38C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-38C>T
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10420
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-23959897-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959897
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959898
    reference: chr 3
allele count: 1
allele frequency: 8.757487651942411e-6
allele num: 114188
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-30dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-30dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-30dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.587dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6957dupT
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-30dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1263dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-30dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-30dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-30dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-30dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-30dupA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-30dupA
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD

3-23959901-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959901
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959901
    reference: chr 3
allele count: 2
allele frequency: 1.742767514813524e-5
allele num: 114760
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-30A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-30A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1263A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6960T>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-30A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-30A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-30A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.587A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-30A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-30A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-30A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-30A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-30A>G
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25927
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11234
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

3-23959906-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959906
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959906
    reference: chr 3
allele count: 8
allele frequency: 6.909775605037227e-5
allele num: 115778
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-25T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-25T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-25T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-25T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1268T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6965A>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-25T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-25T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.592T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-25T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-25T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-25T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-25T>G
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11821
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27202
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-23959907-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959907
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959907
    reference: chr 3
allele count: 275
allele frequency: 2.374292029285813e-3
allele num: 115824
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.593A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1269A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6966T>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-24A>G
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11937
  bin: 2.75e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 6571
  bin: 3.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 3.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27378
  bin: 2.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 4.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2539
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

3-23959909-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959909
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959909
    reference: chr 3
allele count: 1
allele frequency: 8.603334652511313e-6
allele num: 116234
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-22T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-22T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-22T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.595T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6968A>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-22T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-22T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-22T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-22T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-22T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1271T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-22T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-22T>C
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS

3-23959912-CGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959912
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959910
    reference: chr 3
allele count: 2
allele frequency: 1.712886041691646e-5
allele num: 116762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-12_173-11delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6973_-139-6972delAC
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-12_173-11delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-12_*9-11delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1281_1282delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.605_606delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-12_173-11delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-12_173-11delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-12_173-11delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-12_173-11delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-12_173-11delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-12_173-11delGT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-12_173-11delGT
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: CGT
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

3-23959912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959912
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959912
    reference: chr 3
allele count: 4
allele frequency: 3.425772083383293e-5
allele num: 116762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-19C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1274C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-19C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-19C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.598C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-19C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-19C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-19C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-19C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-19C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-19C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6971G>A
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-19C>T
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12332
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

3-23959913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959913
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959913
    reference: chr 3
allele count: 437
allele frequency: 3.726189055065741e-3
allele num: 117278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-18G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-18G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-18G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-18G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-18G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6972C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-18G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-18G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.599G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1275G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-18G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-18G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-18G>A
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 3.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 28287
  bin: 2.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 12431
  bin: 2.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 3.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 4.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
num of homozygotes: 4
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

3-23959913-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959913
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959913
    reference: chr 3
allele count: 4
allele frequency: 3.410699363904569e-5
allele num: 117278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6972C>A
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-18G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-18G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-18G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-18G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-18G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.599G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1275G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-18G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-18G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-18G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-18G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-18G>T
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12431
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

3-23959917-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959917
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959917
    reference: chr 3
allele count: 1
allele frequency: 8.460523198754612e-6
allele num: 118196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6976C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1279G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.603G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-14G>A
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

3-23959919-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959919
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959920
    reference: chr 3
allele count: 1
allele frequency: 8.430708010858751e-6
allele num: 118614
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-9dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1284dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-9dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-9dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-9dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6979dupA
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-9dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-9dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-9dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.608dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-9dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-9dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-9dupT
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

3-23959921-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959921
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959921
    reference: chr 3
allele count: 7
allele frequency: 5.888488845519701e-5
allele num: 118876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-10T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-10T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-10T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-10T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-10T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-10T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6980A>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.607T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1283T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-10T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-10T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-10T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-10T>C
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12947
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29469
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum

3-23959927-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959927
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959927
    reference: chr 3
allele count: 15
allele frequency: 1.251836026171719e-4
allele num: 119824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.173-4G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.173-4G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.173-4G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.173-4G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.173-4G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.173-4G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.173-4G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.173-4G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*9-4G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1289G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6986C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.613G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.173-4G>A
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29976
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13191
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7627
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.173-4G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

3-23959935-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959935
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959935
    reference: chr 3
allele count: 9
allele frequency: 7.482416321644137e-5
allele num: 120282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.177C>T
  hgvsp: ENST00000422218.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.177C>T
  hgvsp: ENST00000412097.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.177C>T
  hgvsp: ENST00000307839.5:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.177C>T
  hgvsp: ENST00000434031.2:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*13C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.177C>T
  hgvsp: ENST00000456530.2:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.177C>T
  hgvsp: ENST00000413699.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.177C>T
  hgvsp: ENST00000415719.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6994G>A
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1297C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.177C>T
  hgvsp: ENST00000354811.5:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.621C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.177C>T
  hgvsp: ENST00000435882.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7791
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr59Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

3-23959936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959936
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959936
    reference: chr 3
allele count: 1
allele frequency: 8.306199747491528e-6
allele num: 120392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.178G>A
  hgvsp: ENSP00000388529.1:p.Val60Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.178G>A
  hgvsp: ENSP00000398788.2:p.Val60Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.178G>A
  hgvsp: ENSP00000387925.1:p.Val60Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.178G>A
  hgvsp: ENSP00000309334.4:p.Val60Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.178G>A
  hgvsp: ENSP00000390193.1:p.Val60Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*14G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.178G>A
  hgvsp: ENSP00000416692.1:p.Val60Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1298G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.622G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.178G>A
  hgvsp: ENSP00000411176.1:p.Val60Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.178G>A
  hgvsp: ENSP00000346867.5:p.Val60Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.178G>A
  hgvsp: ENSP00000405590.2:p.Val60Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6995C>T
  variant of: http://identifiers.org/hgnc/17899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13406
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val60Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

3-23959937-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959937
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959937
    reference: chr 3
allele count: 1
allele frequency: 8.303027283747654e-6
allele num: 120438
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.179T>C
  hgvsp: ENSP00000398788.2:p.Val60Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.179T>C
  hgvsp: ENSP00000309334.4:p.Val60Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*15T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.179T>C
  hgvsp: ENSP00000411176.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.179T>C
  hgvsp: ENSP00000405590.2:p.Val60Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.179T>C
  hgvsp: ENSP00000416692.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.179T>C
  hgvsp: ENSP00000390193.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1299T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-6996A>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.179T>C
  hgvsp: ENSP00000387925.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.179T>C
  hgvsp: ENSP00000388529.1:p.Val60Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.623T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.179T>C
  hgvsp: ENSP00000346867.5:p.Val60Ala
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val60Ala
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-23959954-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959954
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959954
    reference: chr 3
allele count: 4
allele frequency: 3.305020325875004e-5
allele num: 121028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.196G>A
  hgvsp: ENSP00000405590.2:p.Val66Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.196G>A
  hgvsp: ENSP00000309334.4:p.Val66Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7013C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.196G>A
  hgvsp: ENSP00000398788.2:p.Val66Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.196G>A
  hgvsp: ENSP00000390193.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.196G>A
  hgvsp: ENSP00000416692.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.196G>A
  hgvsp: ENSP00000411176.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.640G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.196G>A
  hgvsp: ENSP00000388529.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.196G>A
  hgvsp: ENSP00000387925.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1316G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.196G>A
  hgvsp: ENSP00000346867.5:p.Val66Ile
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val66Ile
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS

3-23959980-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959980
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959980
    reference: chr 3
allele count: 2
allele frequency: 1.649076517150396e-5
allele num: 121280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.222A>G
  hgvsp: ENST00000415719.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*58A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7039T>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.666A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.222A>G
  hgvsp: ENST00000412097.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.222A>G
  hgvsp: ENST00000422218.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.222A>G
  hgvsp: ENST00000434031.2:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.222A>G
  hgvsp: ENST00000354811.5:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.222A>G
  hgvsp: ENST00000307839.5:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.222A>G
  hgvsp: ENST00000456530.2:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1342A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.222A>G
  hgvsp: ENST00000413699.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.222A>G
  hgvsp: ENST00000435882.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro74Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-23959989-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959989
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959989
    reference: chr 3
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.231G>A
  hgvsp: ENST00000415719.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.231G>A
  hgvsp: ENST00000412097.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.231G>A
  hgvsp: ENST00000435882.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.231G>A
  hgvsp: ENST00000354811.5:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.231G>A
  hgvsp: ENST00000456530.2:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.231G>A
  hgvsp: ENST00000413699.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.675G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1351G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.231G>A
  hgvsp: ENST00000434031.2:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.231G>A
  hgvsp: ENST00000422218.1:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.231G>A
  hgvsp: ENST00000307839.5:c.231G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7048C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*67G>A
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8060
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys77Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

3-23959992-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959992
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959992
    reference: chr 3
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.234T>A
  hgvsp: ENST00000354811.5:c.234T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.234T>A
  hgvsp: ENST00000415719.1:c.234T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.678T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*70T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.234T>A
  hgvsp: ENST00000422218.1:c.234T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.234T>A
  hgvsp: ENST00000456530.2:c.234T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.234T>A
  hgvsp: ENST00000412097.1:c.234T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.234T>A
  hgvsp: ENST00000435882.1:c.234T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.234T>A
  hgvsp: ENST00000307839.5:c.234T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.234T>A
  hgvsp: ENST00000413699.1:c.234T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7051A>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1354T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.234T>A
  hgvsp: ENST00000434031.2:c.234T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly78Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-23959998-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23959998
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23959998
    reference: chr 3
allele count: 3
allele frequency: 2.472799208704253e-5
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1360T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.240T>A
  hgvsp: ENST00000422218.1:c.240T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.240T>A
  hgvsp: ENST00000456530.2:c.240T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.240T>A
  hgvsp: ENST00000413699.1:c.240T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7057A>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.240T>A
  hgvsp: ENST00000435882.1:c.240T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.240T>A
  hgvsp: ENST00000307839.5:c.240T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.240T>A
  hgvsp: ENST00000415719.1:c.240T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.240T>A
  hgvsp: ENST00000412097.1:c.240T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.240T>A
  hgvsp: ENST00000354811.5:c.240T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.240T>A
  hgvsp: ENST00000434031.2:c.240T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*76T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.684T>A
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr80Thr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

3-23960001-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960001
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960001
    reference: chr 3
allele count: 295
allele frequency: 2.43162597471109e-3
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.243C>T
  hgvsp: ENST00000307839.5:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.243C>T
  hgvsp: ENST00000434031.2:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.687C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.243C>T
  hgvsp: ENST00000422218.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.243C>T
  hgvsp: ENST00000435882.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.243C>T
  hgvsp: ENST00000415719.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.243C>T
  hgvsp: ENST00000354811.5:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*79C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.243C>T
  hgvsp: ENST00000456530.2:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.243C>T
  hgvsp: ENST00000412097.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.243C>T
  hgvsp: ENST00000413699.1:c.243C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1363C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7060G>A
  variant of: http://identifiers.org/hgnc/17899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 13881
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29779
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8021
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Tyr81Tyr
num of homozygotes: 6
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

3-23960007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960007
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960007
    reference: chr 3
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.249G>A
  hgvsp: ENST00000456530.2:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.693G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.249G>A
  hgvsp: ENST00000307839.5:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.249G>A
  hgvsp: ENST00000354811.5:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.249G>A
  hgvsp: ENST00000422218.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.249G>A
  hgvsp: ENST00000412097.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*85G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.249G>A
  hgvsp: ENST00000413699.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.249G>A
  hgvsp: ENST00000435882.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7066C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.249G>A
  hgvsp: ENST00000434031.2:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1369G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.249G>A
  hgvsp: ENST00000415719.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys83Lys
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

3-23960013-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960013
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960013
    reference: chr 3
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.255C>G
  hgvsp: ENST00000434031.2:c.255C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.699C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.255C>G
  hgvsp: ENST00000415719.1:c.255C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1375C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.255C>G
  hgvsp: ENST00000412097.1:c.255C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.255C>G
  hgvsp: ENST00000413699.1:c.255C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.255C>G
  hgvsp: ENST00000435882.1:c.255C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.255C>G
  hgvsp: ENST00000456530.2:c.255C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.255C>G
  hgvsp: ENST00000307839.5:c.255C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7072G>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*91C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.255C>G
  hgvsp: ENST00000354811.5:c.255C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.255C>G
  hgvsp: ENST00000422218.1:c.255C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 29785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val85Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/3-23960032-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960032
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960032
    reference: chr 3
allele count: 13
allele frequency: 1.071935090207461e-4
allele num: 121276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.274C>A
  hgvsp: ENSP00000411176.1:p.Leu92Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.274C>A
  hgvsp: ENSP00000405590.2:p.Leu92Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.718C>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.274C>A
  hgvsp: ENSP00000388529.1:p.Leu92Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.274C>A
  hgvsp: ENSP00000416692.1:p.Leu92Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7091G>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.274C>A
  hgvsp: ENSP00000346867.5:p.Leu92Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.274C>A
  hgvsp: ENSP00000309334.4:p.Leu92Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.274C>A
  hgvsp: ENSP00000398788.2:p.Leu92Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*110C>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.274C>A
  hgvsp: ENSP00000387925.1:p.Leu92Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1394C>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.274C>A
  hgvsp: ENSP00000390193.1:p.Leu92Ile
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu92Ile
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-23960040-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960040
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960040
    reference: chr 3
allele count: 181
allele frequency: 1.492734260313062e-3
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.282T>C
  hgvsp: ENST00000412097.1:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7099A>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.726T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.282T>C
  hgvsp: ENST00000435882.1:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.282T>C
  hgvsp: ENST00000422218.1:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.282T>C
  hgvsp: ENST00000415719.1:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.282T>C
  hgvsp: ENST00000434031.2:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.282T>C
  hgvsp: ENST00000307839.5:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*118T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.282T>C
  hgvsp: ENST00000456530.2:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.282T>C
  hgvsp: ENST00000413699.1:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.282T>C
  hgvsp: ENST00000354811.5:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1402T>C
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13851
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8028
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 29598
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe94Phe
num of homozygotes: 2
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

3-23960044-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960044
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960044
    reference: chr 3
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.730C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.286C>G
  hgvsp: ENSP00000398788.2:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.286C>G
  hgvsp: ENSP00000416692.1:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.286C>G
  hgvsp: ENSP00000390193.1:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.286C>G
  hgvsp: ENSP00000309334.4:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.286C>G
  hgvsp: ENSP00000387925.1:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.286C>G
  hgvsp: ENSP00000411176.1:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.286C>G
  hgvsp: ENSP00000405590.2:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.286C>G
  hgvsp: ENSP00000388529.1:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1406C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.286C>G
  hgvsp: ENSP00000346867.5:p.Arg96Gly
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*122C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7103G>C
  variant of: http://identifiers.org/hgnc/17899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg96Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

3-23960045-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960045
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960045
    reference: chr 3
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.287G>A
  hgvsp: ENSP00000346867.5:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*123G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.287G>A
  hgvsp: ENSP00000387925.1:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.287G>A
  hgvsp: ENSP00000309334.4:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.731G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.287G>A
  hgvsp: ENSP00000398788.2:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1407G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.287G>A
  hgvsp: ENSP00000416692.1:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7104C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.287G>A
  hgvsp: ENSP00000390193.1:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.287G>A
  hgvsp: ENSP00000405590.2:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.287G>A
  hgvsp: ENSP00000411176.1:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.287G>A
  hgvsp: ENSP00000388529.1:p.Arg96Gln
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg96Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-23960052-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960052
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960052
    reference: chr 3
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.294T>G
  hgvsp: ENST00000412097.1:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.294T>G
  hgvsp: ENST00000434031.2:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.294T>G
  hgvsp: ENST00000435882.1:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1414T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.294T>G
  hgvsp: ENST00000415719.1:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.294T>G
  hgvsp: ENST00000413699.1:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.294T>G
  hgvsp: ENST00000354811.5:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*130T>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.294T>G
  hgvsp: ENST00000456530.2:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.294T>G
  hgvsp: ENST00000307839.5:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.294T>G
  hgvsp: ENST00000422218.1:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7111A>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.738T>G
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu98Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

3-23960056-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960056
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960056
    reference: chr 3
allele count: 1
allele frequency: 8.254230293025175e-6
allele num: 121150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.298T>A
  hgvsp: ENSP00000405590.2:p.Ser100Thr
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.298T>A
  hgvsp: ENSP00000346867.5:p.Ser100Thr
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.298T>A
  hgvsp: ENSP00000388529.1:p.Ser100Thr
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.298T>A
  hgvsp: ENSP00000390193.1:p.Ser100Thr
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.298T>A
  hgvsp: ENSP00000411176.1:p.Ser100Thr
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.298T>A
  hgvsp: ENSP00000416692.1:p.Ser100Thr
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*134T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.298T>A
  hgvsp: ENSP00000398788.2:p.Ser100Thr
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1418T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.298T>A
  hgvsp: ENSP00000309334.4:p.Ser100Thr
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7115A>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.298T>A
  hgvsp: ENSP00000387925.1:p.Ser100Thr
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.742T>A
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser100Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-23960058-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960058
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960058
    reference: chr 3
allele count: 1
allele frequency: 8.256411103221652e-6
allele num: 121118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*136C>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.300C>A
  hgvsp: ENST00000434031.2:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.300C>A
  hgvsp: ENST00000307839.5:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.300C>A
  hgvsp: ENST00000456530.2:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.300C>A
  hgvsp: ENST00000422218.1:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.300C>A
  hgvsp: ENST00000413699.1:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.300C>A
  hgvsp: ENST00000435882.1:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.300C>A
  hgvsp: ENST00000412097.1:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7117G>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.744C>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.300C>A
  hgvsp: ENST00000354811.5:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.300C>A
  hgvsp: ENST00000415719.1:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1420C>A
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser100Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

3-23960058-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960058
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960058
    reference: chr 3
allele count: 3
allele frequency: 2.476923330966496e-5
allele num: 121118
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.300C>G
  hgvsp: ENST00000435882.1:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.744C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.300C>G
  hgvsp: ENST00000422218.1:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.300C>G
  hgvsp: ENST00000412097.1:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*136C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1420C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.300C>G
  hgvsp: ENST00000434031.2:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.300C>G
  hgvsp: ENST00000456530.2:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.300C>G
  hgvsp: ENST00000413699.1:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.300C>G
  hgvsp: ENST00000307839.5:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.300C>G
  hgvsp: ENST00000415719.1:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.300C>G
  hgvsp: ENST00000354811.5:c.300C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7117G>C
  variant of: http://identifiers.org/hgnc/17899
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser100Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

3-23960059-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960059
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960059
    reference: chr 3
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.301G>A
  hgvsp: ENSP00000405590.2:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.301G>A
  hgvsp: ENSP00000390193.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.301G>A
  hgvsp: ENSP00000387925.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*137G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.301G>A
  hgvsp: ENSP00000346867.5:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.745G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.301G>A
  hgvsp: ENSP00000309334.4:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.301G>A
  hgvsp: ENSP00000416692.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.301G>A
  hgvsp: ENSP00000398788.2:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.301G>A
  hgvsp: ENSP00000388529.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1421G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.301G>A
  hgvsp: ENSP00000411176.1:p.Val101Ile
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7118C>T
  variant of: http://identifiers.org/hgnc/17899
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val101Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP

3-23960071-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960071
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960071
    reference: chr 3
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7130T>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+4A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+4A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+4A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+4A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+4A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.313A>G
  hgvsp: ENSP00000411176.1:p.Asn105Asp
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+4A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+4A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+4A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+4A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.757A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+4A>G
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn105Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

3-23960075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960075
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960075
    reference: chr 3
allele count: 2
allele frequency: 1.656314699792961e-5
allele num: 120750
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+8G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+8G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+8G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+8G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.316+1G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7134C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+8G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+8G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+8G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.761G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+8G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+8G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+8G>A
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28766
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.316+1G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

3-23960080-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960080
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960080
    reference: chr 3
allele count: 6596
allele frequency: 5.468957283098965e-2
allele num: 120608
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+13G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+13G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+13G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7139C>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+13G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+13G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+13G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+13G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+13G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.766G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.316+6G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+13G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+13G>C
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.25e1
  variant carriers: 396
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.75e1
  variant carriers: 299
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.25e1
  variant carriers: 232
genotype depth: GenotypeDepth
  all individuals: 7185
  bin: 3.25e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 3.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12333
  bin: 2.75e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 388
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.25e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 8.25e1
  variant carriers: 352
genotype quality: GenotypeQuality
hgvs: c.316+6G>C
num of homozygotes: 408
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

3-23960084-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960084
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960084
    reference: chr 3
allele count: 1
allele frequency: 8.295450774795103e-6
allele num: 120548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+17A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.316+10A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+17A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+17A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+17A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7143T>A
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.770A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+17A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+17A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+17A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+17A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+17A>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+17A>T
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12462
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

3-23960092-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960092
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960092
    reference: chr 3
allele count: 66
allele frequency: 5.485281162214724e-4
allele num: 120322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+25T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+25T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+25T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+25T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+25T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+25T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+25T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+25T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+25T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7151A>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.778T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.316+18T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+25T>C
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12192
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24643
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

3-23960094-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960094
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960094
    reference: chr 3
allele count: 10
allele frequency: 8.313519445321983e-5
allele num: 120286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+27T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+27T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.780T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.316+20T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+27T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+27T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7153A>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+27T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+27T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+27T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+27T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+27T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+27T>C
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

3-23960098-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960098
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960098
    reference: chr 3
allele count: 1
allele frequency: 8.319882856049386e-6
allele num: 120194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7157T>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+31A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+31A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+31A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+31A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+31A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+31A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+31A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+31A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.784A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+31A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.316+24A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+31A>G
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

3-23960117-GGA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960117
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960115
    reference: chr 3
allele count: 2
allele frequency: 1.676980094246281e-5
allele num: 119262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.812_813delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+59_1429+60delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.316+52_316+53delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+59_309+60delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+59_309+60delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+59_309+60delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+59_309+60delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+59_309+60delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7178_-139-7177delTC
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+59_309+60delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+59_309+60delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+59_*145+60delGA
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+59_309+60delGA
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: GGA
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP

3-23960120-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960120
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960120
    reference: chr 3
allele count: 1
allele frequency: 8.394754957102802e-6
allele num: 119122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.316+46G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+53G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+53G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+53G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+53G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+53G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+53G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.806G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+53G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+53G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+53G>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7179C>A
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+53G>T
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

3-23960122-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960122
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960122
    reference: chr 3
allele count: 2
allele frequency: 1.681576646263537e-5
allele num: 118936
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.808G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7181C>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.309+55G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1429+55G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*145+55G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.309+55G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.309+55G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.309+55G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.309+55G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.316+48G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.309+55G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.309+55G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.309+55G>C
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

3-23960637-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960637
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960637
    reference: chr 3
allele count: 1
allele frequency: 8.3558942478024e-6
allele num: 119676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7696A>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.310-50T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1323T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.310-50T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.310-50T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.310-50T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*146-50T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.317-57T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1430-50T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.310-50T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.310-50T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.310-50T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.310-50T>A
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-23960648-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960648
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960648
    reference: chr 3
allele count: 1
allele frequency: 8.351149118118652e-6
allele num: 119744
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.310-39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.310-39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.310-39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.310-39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.310-39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.317-46A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1334A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.310-39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1430-39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7707T>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.310-39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*146-39A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.310-39A>G
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29379
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-23960660-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960660
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960660
    reference: chr 3
allele count: 12
allele frequency: 1.000400160064026e-4
allele num: 119952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.310-27G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.310-27G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*146-27G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.310-27G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.310-27G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7719C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1346G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.317-34G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.310-27G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.310-27G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.310-27G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1430-27G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.310-27G>A
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19076
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29859
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD

3-23960669-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960669
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960669
    reference: chr 3
allele count: 13
allele frequency: 1.081188975199188e-4
allele num: 120238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.310-18C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1355C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.310-18C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.310-18C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7728G>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.310-18C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*146-18C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.310-18C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.310-18C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.310-18C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.317-25C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1430-18C>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.310-18C>G
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19507
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

3-23960670-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960670
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960671
    reference: chr 3
allele count: 1
allele frequency: 8.325285557294615e-6
allele num: 120116
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.310-11dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.310-11dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.310-11dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*146-11dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.317-18dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.310-11dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7730dupA
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1362dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1430-11dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.310-11dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.310-11dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.310-11dupT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.310-11dupT
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

3-23960680-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960680
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960680
    reference: chr 3
allele count: 2
allele frequency: 1.659227795384028e-5
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7739T>C
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.310-7A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.310-7A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.310-7A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1430-7A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.310-7A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.310-7A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.310-7A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*146-7A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.310-7A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1366A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.317-14A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.310-7A>G
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.310-7A>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS

3-23960680-ATTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960680
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960677
    reference: chr 3
allele count: 2
allele frequency: 1.659227795384028e-5
allele num: 120538
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.310-5_310-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.317-12_317-10delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.310-5_310-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.310-5_310-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1430-5_1430-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.310-5_310-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.310-5_310-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*146-5_*146-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7742_-139-7740delGAA
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.310-5_310-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.310-5_310-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.310-5_310-3delTCT
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1368_1370delTCT
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8505
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.310-5_310-3delTCT
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: ATTC
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP

3-23960681-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960681
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960681
    reference: chr 3
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1430-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.310-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.310-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.310-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.310-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*146-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.310-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.310-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.317-13T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.310-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.310-6T>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7740A>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1367T>A
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.310-6T>A
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

3-23960700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960700
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960700
    reference: chr 3
allele count: 6
allele frequency: 4.971002485501243e-5
allele num: 120700
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.323G>A
  hgvsp: ENSP00000398788.2:p.Arg108His
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.323G>A
  hgvsp: ENSP00000390193.1:p.Arg108His
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.323G>A
  hgvsp: ENSP00000309334.4:p.Arg108His
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.323G>A
  hgvsp: ENSP00000416692.1:p.Arg108His
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.323G>A
  hgvsp: ENSP00000405590.2:p.Arg108His
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.323G>A
  hgvsp: ENSP00000346867.5:p.Arg108His
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1443G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.323G>A
  hgvsp: ENSP00000388529.1:p.Arg108His
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7759C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1386G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.323G>A
  hgvsp: ENSP00000411176.1:p.Arg108His
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*159G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.323G>A
  hgvsp: ENSP00000387925.1:p.Arg108His
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19407
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg108His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

3-23960708-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960708
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960708
    reference: chr 3
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1394G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.331G>A
  hgvsp: ENSP00000346867.5:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.331G>A
  hgvsp: ENSP00000411176.1:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1451G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.331G>A
  hgvsp: ENSP00000416692.1:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.331G>A
  hgvsp: ENSP00000309334.4:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.331G>A
  hgvsp: ENSP00000388529.1:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.331G>A
  hgvsp: ENSP00000390193.1:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.331G>A
  hgvsp: ENSP00000398788.2:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.331G>A
  hgvsp: ENSP00000387925.1:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*167G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7767C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.331G>A
  hgvsp: ENSP00000405590.2:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly111Arg
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

3-23960709-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960709
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960709
    reference: chr 3
allele count: 1
allele frequency: 8.286651861182008e-6
allele num: 120676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.332G>C
  hgvsp: ENSP00000411176.1:p.Gly111Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.332G>C
  hgvsp: ENSP00000416692.1:p.Gly111Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.332G>C
  hgvsp: ENSP00000398788.2:p.Gly111Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.332G>C
  hgvsp: ENSP00000405590.2:p.Gly111Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*168G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.332G>C
  hgvsp: ENSP00000346867.5:p.Gly111Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.332G>C
  hgvsp: ENSP00000388529.1:p.Gly111Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.332G>C
  hgvsp: ENSP00000387925.1:p.Gly111Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.332G>C
  hgvsp: ENSP00000309334.4:p.Gly111Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1452G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7768C>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1395G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.332G>C
  hgvsp: ENSP00000390193.1:p.Gly111Ala
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly111Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

3-23960716-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960716
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960716
    reference: chr 3
allele count: 12
allele frequency: 9.946619807035576e-5
allele num: 120644
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.339G>C
  hgvsp: ENST00000456530.2:c.339G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.339G>C
  hgvsp: ENST00000415719.1:c.339G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7775C>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.339G>C
  hgvsp: ENST00000435882.1:c.339G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*175G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.339G>C
  hgvsp: ENST00000354811.5:c.339G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.339G>C
  hgvsp: ENST00000434031.2:c.339G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.339G>C
  hgvsp: ENST00000307839.5:c.339G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1459G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.339G>C
  hgvsp: ENST00000412097.1:c.339G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.339G>C
  hgvsp: ENST00000413699.1:c.339G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1402G>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.339G>C
  hgvsp: ENST00000422218.1:c.339G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Leu113Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

3-23960718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960718
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960718
    reference: chr 3
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.341G>A
  hgvsp: ENSP00000346867.5:p.Arg114Lys
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.341G>A
  hgvsp: ENSP00000390193.1:p.Arg114Lys
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.341G>A
  hgvsp: ENSP00000398788.2:p.Arg114Lys
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.341G>A
  hgvsp: ENSP00000388529.1:p.Arg114Lys
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1461G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7777C>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.341G>A
  hgvsp: ENSP00000411176.1:p.Arg114Lys
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*177G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.341G>A
  hgvsp: ENSP00000387925.1:p.Arg114Lys
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.341G>A
  hgvsp: ENSP00000416692.1:p.Arg114Lys
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1404G>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.341G>A
  hgvsp: ENSP00000309334.4:p.Arg114Lys
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.341G>A
  hgvsp: ENSP00000405590.2:p.Arg114Lys
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8505
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg114Lys
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/3-23960722-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960722
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960722
    reference: chr 3
allele count: 2
allele frequency: 1.658787426391308e-5
allele num: 120570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7781G>T
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.345C>A
  hgvsp: ENST00000412097.1:c.345C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.345C>A
  hgvsp: ENST00000434031.2:c.345C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.345C>A
  hgvsp: ENST00000413699.1:c.345C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.345C>A
  hgvsp: ENST00000415719.1:c.345C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.345C>A
  hgvsp: ENST00000435882.1:c.345C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.345C>A
  hgvsp: ENST00000456530.2:c.345C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.345C>A
  hgvsp: ENST00000422218.1:c.345C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1465C>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.345C>A
  hgvsp: ENST00000307839.5:c.345C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*181C>A
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.345C>A
  hgvsp: ENST00000354811.5:c.345C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1408C>A
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val115Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-23960740-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960740
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960740
    reference: chr 3
allele count: 3
allele frequency: 2.497003595685178e-5
allele num: 120144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.363T>C
  hgvsp: ENST00000354811.5:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.363T>C
  hgvsp: ENST00000415719.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.363T>C
  hgvsp: ENST00000422218.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1426T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.363T>C
  hgvsp: ENST00000435882.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.363T>C
  hgvsp: ENST00000412097.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.360+3T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.363T>C
  hgvsp: ENST00000413699.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*199T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.363T>C
  hgvsp: ENST00000307839.5:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1483T>C
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7799A>G
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.363T>C
  hgvsp: ENST00000434031.2:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.360+3T>C
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

3-23960753-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960753
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960753
    reference: chr 3
allele count: 1
allele frequency: 8.355614973262032e-6
allele num: 119680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.376A>G
  hgvsp: ENSP00000387925.1:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1496A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.376A>G
  hgvsp: ENSP00000416692.1:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.376A>G
  hgvsp: ENSP00000346867.5:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*212A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.376A>G
  hgvsp: ENSP00000388529.1:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.360+16A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1439A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.376A>G
  hgvsp: ENSP00000405590.2:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.376A>G
  hgvsp: ENSP00000390193.1:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.376A>G
  hgvsp: ENSP00000309334.4:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.376A>G
  hgvsp: ENSP00000411176.1:p.Thr126Ala
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7812T>C
  variant of: http://identifiers.org/hgnc/17899
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr126Ala
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

3-23960758-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960758
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960758
    reference: chr 3
allele count: 6
allele frequency: 5.022685797518794e-5
allele num: 119458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.360+21C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1501C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7817G>A
  variant of: http://identifiers.org/hgnc/17899
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.381C>T
  hgvsp: ENST00000434031.2:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.381C>T
  hgvsp: ENST00000435882.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.381C>T
  hgvsp: ENST00000354811.5:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*217C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.381C>T
  hgvsp: ENST00000422218.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.381C>T
  hgvsp: ENST00000413699.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.381C>T
  hgvsp: ENST00000412097.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.381C>T
  hgvsp: ENST00000415719.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1444C>T
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.381C>T
  hgvsp: ENST00000307839.5:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10306
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr127Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

3-23960760-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 23960760
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 23960760
    reference: chr 3
allele count: 4
allele frequency: 3.350083752093803e-5
allele num: 119400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000405590
  ensembl transcript: ENST00000434031
  gene symbol: RPL15
  hgvsc: ENST00000434031.2:c.383A>G
  hgvsp: ENSP00000405590.2:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000490223
  gene symbol: RPL15
  hgvsc: ENST00000490223.1:n.1503A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000309334
  ensembl transcript: ENST00000307839
  gene symbol: RPL15
  hgvsc: ENST00000307839.5:c.383A>G
  hgvsp: ENSP00000309334.4:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000346867
  ensembl transcript: ENST00000354811
  gene symbol: RPL15
  hgvsc: ENST00000354811.5:c.383A>G
  hgvsp: ENSP00000346867.5:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000390193
  ensembl transcript: ENST00000435882
  gene symbol: RPL15
  hgvsc: ENST00000435882.1:c.383A>G
  hgvsp: ENSP00000390193.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000388529
  ensembl transcript: ENST00000415719
  gene symbol: RPL15
  hgvsc: ENST00000415719.1:c.383A>G
  hgvsp: ENSP00000388529.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000408243
  ensembl transcript: ENST00000436146
  gene symbol: RPL15
  hgvsc: ENST00000436146.1:c.*219A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174748
  ensembl transcript: ENST00000465786
  gene symbol: RPL15
  hgvsc: ENST00000465786.1:n.1446A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000398788
  ensembl transcript: ENST00000456530
  gene symbol: RPL15
  hgvsc: ENST00000456530.2:c.360+23A>G
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000387925
  ensembl transcript: ENST00000422218
  gene symbol: RPL15
  hgvsc: ENST00000422218.1:c.383A>G
  hgvsp: ENSP00000387925.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000416692
  ensembl transcript: ENST00000413699
  gene symbol: RPL15
  hgvsc: ENST00000413699.1:c.383A>G
  hgvsp: ENSP00000416692.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174748
  ensembl protein: ENSP00000411176
  ensembl transcript: ENST00000412097
  gene symbol: RPL15
  hgvsc: ENST00000412097.1:c.383A>G
  hgvsp: ENSP00000411176.1:p.Lys128Arg
  variant of: http://identifiers.org/hgnc/10306
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000197885
  ensembl protein: ENSP00000392307
  ensembl transcript: ENST00000421515
  gene symbol: NKIRAS1
  hgvsc: ENST00000421515.2:c.-139-7819T>C
  variant of: http://identifiers.org/hgnc/17899
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8374
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30591
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys128Arg
num of homozygotes: 0
population: East Asian
reference allele: A

GenotypeDepth
all individuals: 79
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 70
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 289
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5887
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5960
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1959
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4686
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6354
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6812
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4082
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.60498186370494e-5
allele num: 62306
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.02e0

DP
type: SiteQuality
SIO_000300: 1.399878e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

QD
type: SiteQuality
SIO_000300: 1.048e1

VQSLOD
type: SiteQuality
SIO_000300: -3.548e0

FS
type: SiteQuality
SIO_000300: 4.465e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.254e0

MQRankSum
type: SiteQuality
SIO_000300: -1.435e0

MQ
type: SiteQuality
SIO_000300: 5.476e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

GenotypeDepth
all individuals: 1447
bin: 9.75e1
variant carriers: 47

GenotypeDepth
all individuals: 123
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 2251
bin: 3.75e1
variant carriers: 57

GenotypeQuality
all individuals: 1547
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3343
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 8470
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 874
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5269
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 277
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 3983
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2077
bin: 8.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2894
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4773
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2720
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4815
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 4940
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 461
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 7250
bin: 9.75e1
variant carriers: 1348

GenotypeQuality
all individuals: 930
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1250
bin: 9.25e1
variant carriers: 13

GenotypeQuality
all individuals: 2224
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7776
num of homozygotes: 0

Latino
type: Population
allele count: 18
allele frequency: 1.701644923425978e-3
allele num: 10578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 92
allele frequency: 1.425914445133292e-2
allele num: 6452
num of homozygotes: 1

African
type: Population
allele count: 34
allele frequency: 3.495065789473684e-3
allele num: 9728
num of homozygotes: 0

South Asian
type: Population
allele count: 27
allele frequency: 1.799520127965876e-3
allele num: 15004
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1207
allele frequency: 1.933365369213519e-2
allele num: 62430
num of homozygotes: 12

Other
type: Population
allele count: 6
allele frequency: 7.125890736342043e-3
allele num: 842
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.32e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

VQSLOD
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SIO_000300: 3.9e-1

InbreedingCoeff
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SIO_000300: 6.0e-3

QD
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SIO_000300: 1.472e1

DP
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SIO_000300: 1.556132e6

ReadPosRankSum
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SIO_000300: 2.59e-1

BaseQRankSum
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SIO_000300: -2.489e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.602410024677114e-5
allele num: 62406
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14936
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.393e0

VQSLOD
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DP
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InbreedingCoeff
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SIO_000300: -1.4e-3

ClippingRankSum
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MQ
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SIO_000300: 5.707e1

BaseQRankSum
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MQRankSum
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SIO_000300: 6.94e-1

QD
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SIO_000300: 5.6e0

ReadPosRankSum
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SIO_000300: 6.850000000000001e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 2405
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10736
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.59108884787767e-5
allele num: 15172
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62950
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.62883e6

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
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BaseQRankSum
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SIO_000300: 1.33e0

ClippingRankSum
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SIO_000300: 2.83e-1

MQRankSum
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SIO_000300: 8.79e-1

FS
type: SiteQuality
SIO_000300: 5.19e-1

QD
type: SiteQuality
SIO_000300: 1.586e1

MQ
type: SiteQuality
SIO_000300: 5.776e1

VQSLOD
type: SiteQuality
SIO_000300: 2.74e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6098
bin: 9.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62768
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.244e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

FS
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SIO_000300: 5.0624e1

QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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SIO_000300: -5.86e-1

DP
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SIO_000300: 1.636923e6

BaseQRankSum
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SIO_000300: -2.219e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.274717121127805e-5
allele num: 10782
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63130
num of homozygotes: 0

VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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SIO_000300: 5.197e1

QD
type: SiteQuality
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GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.153479865031062e-5
allele num: 63422
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeDepth
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variant carriers: 2

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63932
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
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11032
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.074283407347598e-4
allele num: 9908
num of homozygotes: 0

South Asian
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allele count: 0
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MQRankSum
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SIO_000300: 6.6e-2

InbreedingCoeff
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FS
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DP
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BaseQRankSum
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MQ
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -2.36e-1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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variant carriers: 14

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 270

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10
allele frequency: 6.466632177961717e-4
allele num: 15464
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.28310502283105e-3
allele num: 876
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.016942315449778e-4
allele num: 9916
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63938
num of homozygotes: 0

East Asian
type: Population
allele count: 122
allele frequency: 1.514023330851328e-2
allele num: 8058
num of homozygotes: 1

Latino
type: Population
allele count: 139
allele frequency: 1.257690915671372e-2
allele num: 11052
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.66e-1

MQ
type: SiteQuality
SIO_000300: 5.328e1

DP
type: SiteQuality
SIO_000300: 1.738813e6

QD
type: SiteQuality
SIO_000300: 1.523e1

GenotypeDepth
all individuals: 1436
bin: 9.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27679
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559478510386127e-5
allele num: 64124
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.368e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQRankSum
type: SiteQuality
SIO_000300: -4.09e-1

MQ
type: SiteQuality
SIO_000300: 5.329e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.952e0

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e0

DP
type: SiteQuality
SIO_000300: 1.749543e6

FS
type: SiteQuality
SIO_000300: 2.823e0

GenotypeDepth
all individuals: 2008
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3804
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variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8186
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.002402883460152e-4
allele num: 9988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11156
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.76662e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.86e0

QD
type: SiteQuality
SIO_000300: 1.526e1

ClippingRankSum
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.382e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.027e0

MQ
type: SiteQuality
SIO_000300: 5.398e1

GenotypeDepth
all individuals: 147
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1436
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 75
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1214
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variant carriers: 0

GenotypeQuality
all individuals: 421
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variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8186
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.210408644888833e-5
allele num: 64408
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.382e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.86e0

DP
type: SiteQuality
SIO_000300: 1.76662e6

MQ
type: SiteQuality
SIO_000300: 5.398e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.027e0

QD
type: SiteQuality
SIO_000300: 1.526e1

GenotypeDepth
all individuals: 141
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 141
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variant carriers: 3

GenotypeDepth
all individuals: 122
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variant carriers: 3

GenotypeQuality
all individuals: 255
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GenotypeQuality
all individuals: 2296
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GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 7135
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variant carriers: 0

GenotypeQuality
all individuals: 1252
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variant carriers: 0

GenotypeQuality
all individuals: 669
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variant carriers: 1

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 673
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variant carriers: 1

GenotypeQuality
all individuals: 551
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variant carriers: 0

GenotypeQuality
all individuals: 564
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variant carriers: 1

GenotypeQuality
all individuals: 27825
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variant carriers: 1

GenotypeQuality
all individuals: 2902
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6742
bin: 9.75e1
variant carriers: 429

GenotypeQuality
all individuals: 21
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GenotypeQuality
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GenotypeQuality
all individuals: 3053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 298
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.628928898382667e-4
allele num: 6554
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 7.139032661074424e-4
allele num: 11206
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 1.694577352472089e-3
allele num: 10032
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.133786848072562e-3
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 83
allele frequency: 5.285277636271014e-3
allele num: 15704
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 323
allele frequency: 4.99412455934195e-3
allele num: 64676
num of homozygotes: 3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

FS
type: SiteQuality
SIO_000300: 7.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 5.373e1

QD
type: SiteQuality
SIO_000300: 1.355e1

DP
type: SiteQuality
SIO_000300: 1.778818e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

GenotypeDepth
all individuals: 141
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 150
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variant carriers: 1

GenotypeDepth
all individuals: 206
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GenotypeQuality
all individuals: 43
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 21
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GenotypeQuality
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GenotypeQuality
all individuals: 829
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GenotypeQuality
all individuals: 2902
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 298
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6742
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 673
bin: 5.75e1
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GenotypeQuality
all individuals: 3971
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GenotypeQuality
all individuals: 1252
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variant carriers: 0

GenotypeQuality
all individuals: 3053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.184674376894056e-5
allele num: 64676
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.6e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

MQ
type: SiteQuality
SIO_000300: 5.373e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

DP
type: SiteQuality
SIO_000300: 1.778818e6

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

GenotypeDepth
all individuals: 149
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variant carriers: 0

GenotypeDepth
all individuals: 142
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GenotypeDepth
all individuals: 177
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 93
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GenotypeQuality
all individuals: 24
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65154
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.201923076923077e-4
allele num: 8320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-1

MQ
type: SiteQuality
SIO_000300: 5.307e1

DP
type: SiteQuality
SIO_000300: 1.79557e6

FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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SIO_000300: 3.5e-3

BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.415e1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4156
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65360
num of homozygotes: 0

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

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

Latino
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allele frequency: 8.804366966015144e-5
allele num: 11358
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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BaseQRankSum
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SIO_000300: -5.37e-1

ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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QD
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MQ
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.068571777492825e-4
allele num: 65508
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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African
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South Asian
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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QD
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65964
num of homozygotes: 0

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

African
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East Asian
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Other
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allele num: 900
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South Asian
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allele count: 15
allele frequency: 9.31214303451701e-4
allele num: 16108
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -3.594e0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10310
num of homozygotes: 0

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

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

East Asian
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allele count: 5
allele frequency: 5.841121495327102e-4
allele num: 8560
num of homozygotes: 0

Latino
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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: 902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.043391551338611e-5
allele num: 66188
num of homozygotes: 0

InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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DP
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FS
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SIO_000300: 1.559e0

BaseQRankSum
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SIO_000300: -3.062e0

ReadPosRankSum
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SIO_000300: 7.45e-1

ClippingRankSum
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SIO_000300: -8.33e-1

QD
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SIO_000300: 1.389e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.50952510340247e-5
allele num: 66246
num of homozygotes: 0

Other
type: Population
allele count: 0
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Latino
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allele frequency: 0.0e0
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African
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East Asian
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European (Finnish)
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South Asian
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QD
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VQSLOD
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MQRankSum
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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Other
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East Asian
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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FS
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QD
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DP
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MQRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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East Asian
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VQSLOD
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MQ
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Latino
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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DP
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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African
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Latino
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Other
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East Asian
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South Asian
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66692
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East Asian
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European (Finnish)
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South Asian
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Latino
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African
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Other
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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DP
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 9.52e-1

MQRankSum
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QD
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 8.9e-3

FS
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.073858114674441e-5
allele num: 16464
num of homozygotes: 0

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

Latino
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allele count: 6
allele frequency: 5.183137525915688e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 8.998740176375308e-5
allele num: 66676
num of homozygotes: 0

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

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

QD
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InbreedingCoeff
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ClippingRankSum
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MQ
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DP
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MQRankSum
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VQSLOD
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FS
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SIO_000300: 1.773e0

ReadPosRankSum
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SIO_000300: 5.92e-1

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

Latino
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allele count: 4
allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

South Asian
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allele count: 132
allele frequency: 8.020415603353991e-3
allele num: 16458
num of homozygotes: 1

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

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

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

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

European (Non-Finnish)
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allele count: 45
allele frequency: 6.750067500675006e-4
allele num: 66666
num of homozygotes: 1

BaseQRankSum
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SIO_000300: -1.029e0

DP
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SIO_000300: 1.869083e6

MQ
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SIO_000300: 4.596e1

MQRankSum
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QD
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FS
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ClippingRankSum
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SIO_000300: 7.8e-2

InbreedingCoeff
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SIO_000300: 2.15e-2

VQSLOD
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SIO_000300: -5.093e-1

ReadPosRankSum
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SIO_000300: 4.71e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

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

East Asian
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allele count: 0
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ReadPosRankSum
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SIO_000300: 2.63e-1

BaseQRankSum
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DP
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FS
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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SIO_000300: 3.58e-1

MQ
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SIO_000300: 4.714e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

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

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

East Asian
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Other
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 66648
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Other
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African
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South Asian
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East Asian
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Latino
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European (Finnish)
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FS
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Non-Finnish)
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African
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Other
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South Asian
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European (Finnish)
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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QD
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VQSLOD
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

South Asian
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allele frequency: 1.831501831501832e-4
allele num: 16380
num of homozygotes: 0

MQRankSum
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SIO_000300: 3.45e-1

ClippingRankSum
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QD
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FS
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InbreedingCoeff
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MQ
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VQSLOD
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BaseQRankSum
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SIO_000300: 2.64e0

ReadPosRankSum
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DP
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SIO_000300: 1.85985e6

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.109481915933529e-5
allele num: 16368
num of homozygotes: 0

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

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

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

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

VQSLOD
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SIO_000300: -1.693e0

ReadPosRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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SIO_000300: 8.191000000000001e0

MQ
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SIO_000300: 5.051e1

MQRankSum
type: SiteQuality
SIO_000300: 9.63e-1

DP
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SIO_000300: 1.859085e6

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16204
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
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allele num: 8654
num of homozygotes: 0

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

MQ
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SIO_000300: 5.286e1

MQRankSum
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SIO_000300: 1.42e0

ClippingRankSum
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SIO_000300: -2.38e-1

QD
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
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SIO_000300: 9.561e0

BaseQRankSum
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SIO_000300: 6.32e0

DP
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SIO_000300: 1.852614e6

VQSLOD
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SIO_000300: -1.766e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-1

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.005259203606311e-5
allele num: 66550
num of homozygotes: 0

BaseQRankSum
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ClippingRankSum
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QD
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VQSLOD
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FS
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SIO_000300: 4.587e0

MQRankSum
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SIO_000300: 9.55e-1

MQ
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SIO_000300: 5.311e1

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.22e-1

DP
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SIO_000300: 1.849522e6

GenotypeDepth
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variant carriers: 66

GenotypeDepth
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variant carriers: 3592

GenotypeDepth
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variant carriers: 113

GenotypeDepth
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variant carriers: 175

GenotypeQuality
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GenotypeQuality
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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: 6173

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1253
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Latino
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allele count: 1010
allele frequency: 8.726455849317435e-2
allele num: 11574
num of homozygotes: 49

South Asian
type: Population
allele count: 407
allele frequency: 2.532354405176705e-2
allele num: 16072
num of homozygotes: 10

African
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allele count: 172
allele frequency: 1.67055167055167e-2
allele num: 10296
num of homozygotes: 1

European (Finnish)
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allele count: 295
allele frequency: 4.46023586332023e-2
allele num: 6614
num of homozygotes: 6

Other
type: Population
allele count: 58
allele frequency: 6.45879732739421e-2
allele num: 898
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European (Non-Finnish)
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allele count: 2395
allele frequency: 3.599879753494664e-2
allele num: 66530
num of homozygotes: 50

East Asian
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allele count: 2259
allele frequency: 2.61943413729128e-1
allele num: 8624
num of homozygotes: 289

MQ
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SIO_000300: 5.169e1

FS
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SIO_000300: 6.12e-1

QD
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DP
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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SIO_000300: 1.88e0

MQRankSum
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SIO_000300: 4.17e-1

ClippingRankSum
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SIO_000300: -2.82e-1

BaseQRankSum
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SIO_000300: 1.14e0

GenotypeDepth
all individuals: 725
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

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

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

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

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

South Asian
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allele frequency: 6.243756243756244e-5
allele num: 16016
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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DP
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SIO_000300: 1.99917e6

ClippingRankSum
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SIO_000300: 2.8e-1

ReadPosRankSum
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SIO_000300: 7.0e-3

MQ
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SIO_000300: 5.699e1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66472
num of homozygotes: 0

African
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allele num: 10242
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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Other
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South Asian
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allele frequency: 4.030734349414284e-3
allele num: 15878
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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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European (Finnish)
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allele num: 6614
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South Asian
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allele num: 15850
num of homozygotes: 0

East Asian
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Other
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Latino
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FS
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -2.92e-1

InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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QD
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SIO_000300: 1.624e1

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

South Asian
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allele count: 1
allele frequency: 6.322711178553364e-5
allele num: 15816
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66442
num of homozygotes: 0

African
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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

Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.724e1

BaseQRankSum
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SIO_000300: 3.66e0

DP
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: 1.07e0

GenotypeDepth
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variant carriers: 1

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

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

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

Latino
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num of homozygotes: 0

African
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Other
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.021421881137263e-5
allele num: 66194
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South Asian
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ClippingRankSum
type: SiteQuality
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VQSLOD
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele num: 66150
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European (Finnish)
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African
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Latino
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East Asian
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Other
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South Asian
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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FS
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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African
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ReadPosRankSum
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VQSLOD
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MQ
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MQRankSum
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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South Asian
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allele num: 15930
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European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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QD
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9836
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

European (Finnish)
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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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East Asian
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allele frequency: 0.0e0
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South Asian
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Other
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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QD
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FS
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MQ
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 12

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

East Asian
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allele frequency: 4.673989249824726e-4
allele num: 8558
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 8
allele frequency: 1.204492757987293e-4
allele num: 66418
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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InbreedingCoeff
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SIO_000300: 4.1e-3

BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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MQ
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FS
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SIO_000300: 0.0e0

QD
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VQSLOD
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SIO_000300: 2.1e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 11
allele frequency: 1.654035847467821e-4
allele num: 66504
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
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European (Finnish)
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allele count: 2
allele frequency: 3.024803387779795e-4
allele num: 6612
num of homozygotes: 0

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

Other
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allele num: 902
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European (Finnish)
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African
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South Asian
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Latino
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European (Non-Finnish)
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ReadPosRankSum
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DP
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FS
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQ
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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Latino
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European (Non-Finnish)
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Other
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European (Finnish)
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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InbreedingCoeff
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DP
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VQSLOD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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European (Finnish)
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African
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South Asian
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Latino
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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QD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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MQ
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FS
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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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Other
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African
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South Asian
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European (Finnish)
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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East Asian
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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QD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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South Asian
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East Asian
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MQ
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FS
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QD
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BaseQRankSum
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

African
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Latino
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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MQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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East Asian
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QD
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VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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MQRankSum
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DP
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FS
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QD
type: SiteQuality
SIO_000300: 2.881e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 4.4e1

VQSLOD
type: SiteQuality
SIO_000300: -1.334e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.993e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 24
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66346
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.604618857440528e-4
allele num: 11518
num of homozygotes: 0

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

East Asian
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allele count: 0
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BaseQRankSum
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SIO_000300: -1.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
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SIO_000300: 1.3e0

VQSLOD
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SIO_000300: -2.309e0

DP
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SIO_000300: 1.579715e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

FS
type: SiteQuality
SIO_000300: 8.054e0

MQ
type: SiteQuality
SIO_000300: 4.553e1

QD
type: SiteQuality
SIO_000300: 1.127e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.512813530604218e-5
allele num: 66102
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.082e0

MQ
type: SiteQuality
SIO_000300: 4.557e1

BaseQRankSum
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SIO_000300: 5.17e0

FS
type: SiteQuality
SIO_000300: 3.506e0

MQRankSum
type: SiteQuality
SIO_000300: -1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e0

QD
type: SiteQuality
SIO_000300: 1.041e1

VQSLOD
type: SiteQuality
SIO_000300: -2.685e0

DP
type: SiteQuality
SIO_000300: 1.572939e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

African
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allele count: 6
allele frequency: 6.234413965087282e-4
allele num: 9624
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65966
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: 1.0e-4

MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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SIO_000300: -1.42e-1

MQ
type: SiteQuality
SIO_000300: 4.192e1

FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.11e-1

BaseQRankSum
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SIO_000300: -3.582e0

DP
type: SiteQuality
SIO_000300: 1.570032e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 52
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GenotypeQuality
all individuals: 141
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variant carriers: 0

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