11-502178-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502178
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502178
    reference: chr 11
allele count: 1
allele frequency: 1.342606267286056e-5
allele num: 74482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435798
  ensembl transcript: ENST00000531149
  gene symbol: RNH1
  hgvsc: ENST00000531149.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433033
  ensembl transcript: ENST00000529115
  gene symbol: RNH1
  hgvsc: ENST00000529115.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000533592
  gene symbol: RNH1
  hgvsc: ENST00000533592.1:n.1006A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.328A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435594
  ensembl transcript: ENST00000533410
  gene symbol: RNH1
  hgvsc: ENST00000533410.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.38A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000346402
  ensembl transcript: ENST00000354420
  gene symbol: RNH1
  hgvsc: ENST00000354420.2:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380738
  ensembl transcript: ENST00000397614
  gene symbol: RNH1
  hgvsc: ENST00000397614.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000416589
  ensembl transcript: ENST00000438658
  gene symbol: RNH1
  hgvsc: ENST00000438658.2:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000431201
  ensembl transcript: ENST00000524464
  gene symbol: RNH1
  hgvsc: ENST00000524464.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-16A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.172A>G
  variant of: http://identifiers.org/hgnc/10074
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP

11-502179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502179
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502179
    reference: chr 11
allele count: 1
allele frequency: 1.358289641683193e-5
allele num: 73622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000416589
  ensembl transcript: ENST00000438658
  gene symbol: RNH1
  hgvsc: ENST00000438658.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435798
  ensembl transcript: ENST00000531149
  gene symbol: RNH1
  hgvsc: ENST00000531149.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.37C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.327C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433033
  ensembl transcript: ENST00000529115
  gene symbol: RNH1
  hgvsc: ENST00000529115.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000346402
  ensembl transcript: ENST00000354420
  gene symbol: RNH1
  hgvsc: ENST00000354420.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435594
  ensembl transcript: ENST00000533410
  gene symbol: RNH1
  hgvsc: ENST00000533410.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.171C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000431201
  ensembl transcript: ENST00000524464
  gene symbol: RNH1
  hgvsc: ENST00000524464.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000525522
  gene symbol: RNH1
  hgvsc: ENST00000525522.1:n.1061C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/10074
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.-17C>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-502196-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502196
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502196
    reference: chr 11
allele count: 1
allele frequency: 1.670564650851988e-5
allele num: 59860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-34C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000416589
  ensembl transcript: ENST00000438658
  gene symbol: RNH1
  hgvsc: ENST00000438658.2:c.-19-15C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380738
  ensembl transcript: ENST00000397614
  gene symbol: RNH1
  hgvsc: ENST00000397614.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-19-15C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000346402
  ensembl transcript: ENST00000354420
  gene symbol: RNH1
  hgvsc: ENST00000354420.2:c.-34C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433033
  ensembl transcript: ENST00000529115
  gene symbol: RNH1
  hgvsc: ENST00000529115.1:c.-19-15C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-34C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-19-15C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000525522
  gene symbol: RNH1
  hgvsc: ENST00000525522.1:n.1059-15C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.20C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.310C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000533592
  gene symbol: RNH1
  hgvsc: ENST00000533592.1:n.988C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000431201
  ensembl transcript: ENST00000524464
  gene symbol: RNH1
  hgvsc: ENST00000524464.1:c.-19-15C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-19-15C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.154C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435798
  ensembl transcript: ENST00000531149
  gene symbol: RNH1
  hgvsc: ENST00000531149.1:c.-19-15C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-34C>T
  variant of: http://identifiers.org/hgnc/10074
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-502198-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502198
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502198
    reference: chr 11
allele count: 1
allele frequency: 1.671849399806065e-5
allele num: 59814
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.308C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.152C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-19-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000346402
  ensembl transcript: ENST00000354420
  gene symbol: RNH1
  hgvsc: ENST00000354420.2:c.-36C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-36C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435594
  ensembl transcript: ENST00000533410
  gene symbol: RNH1
  hgvsc: ENST00000533410.1:c.-19-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-19-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-36C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380738
  ensembl transcript: ENST00000397614
  gene symbol: RNH1
  hgvsc: ENST00000397614.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.18C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-19-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000533592
  gene symbol: RNH1
  hgvsc: ENST00000533592.1:n.986C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000525522
  gene symbol: RNH1
  hgvsc: ENST00000525522.1:n.1059-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000431201
  ensembl transcript: ENST00000524464
  gene symbol: RNH1
  hgvsc: ENST00000524464.1:c.-19-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000416589
  ensembl transcript: ENST00000438658
  gene symbol: RNH1
  hgvsc: ENST00000438658.2:c.-19-17C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-36C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433033
  ensembl transcript: ENST00000529115
  gene symbol: RNH1
  hgvsc: ENST00000529115.1:c.-19-17C>T
  variant of: http://identifiers.org/hgnc/10074
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-502204-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502204
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502204
    reference: chr 11
allele count: 119
allele frequency: 2.212224866151101e-3
allele num: 53792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-42T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-19-23T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-42T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.302T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-19-23T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.12T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433033
  ensembl transcript: ENST00000529115
  gene symbol: RNH1
  hgvsc: ENST00000529115.1:c.-19-23T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000416589
  ensembl transcript: ENST00000438658
  gene symbol: RNH1
  hgvsc: ENST00000438658.2:c.-19-23T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-42T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-42T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435798
  ensembl transcript: ENST00000531149
  gene symbol: RNH1
  hgvsc: ENST00000531149.1:c.-19-23T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-42T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-42T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000431201
  ensembl transcript: ENST00000524464
  gene symbol: RNH1
  hgvsc: ENST00000524464.1:c.-19-23T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380738
  ensembl transcript: ENST00000397614
  gene symbol: RNH1
  hgvsc: ENST00000397614.1:c.-42T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.146T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-42T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000346402
  ensembl transcript: ENST00000354420
  gene symbol: RNH1
  hgvsc: ENST00000354420.2:c.-42T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000525522
  gene symbol: RNH1
  hgvsc: ENST00000525522.1:n.1059-23T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435594
  ensembl transcript: ENST00000533410
  gene symbol: RNH1
  hgvsc: ENST00000533410.1:c.-19-23T>C
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-19-23T>C
  variant of: http://identifiers.org/hgnc/10074
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

11-502206-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502206
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502206
    reference: chr 11
allele count: 1
allele frequency: 1.955110659263314e-5
allele num: 51148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-19-25C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-44C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-44C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-44C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435594
  ensembl transcript: ENST00000533410
  gene symbol: RNH1
  hgvsc: ENST00000533410.1:c.-19-25C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.300C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-44C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-44C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-44C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-19-25C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435798
  ensembl transcript: ENST00000531149
  gene symbol: RNH1
  hgvsc: ENST00000531149.1:c.-19-25C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-19-25C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000533592
  gene symbol: RNH1
  hgvsc: ENST00000533592.1:n.978C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.10C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.144C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380738
  ensembl transcript: ENST00000397614
  gene symbol: RNH1
  hgvsc: ENST00000397614.1:c.-44C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000525522
  gene symbol: RNH1
  hgvsc: ENST00000525522.1:n.1059-25C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000416589
  ensembl transcript: ENST00000438658
  gene symbol: RNH1
  hgvsc: ENST00000438658.2:c.-19-25C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-44C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000431201
  ensembl transcript: ENST00000524464
  gene symbol: RNH1
  hgvsc: ENST00000524464.1:c.-19-25C>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433033
  ensembl transcript: ENST00000529115
  gene symbol: RNH1
  hgvsc: ENST00000529115.1:c.-19-25C>A
  variant of: http://identifiers.org/hgnc/10074
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

11-502208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502208
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502208
    reference: chr 11
allele count: 3
allele frequency: 6.320846150604694e-5
allele num: 47462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000416589
  ensembl transcript: ENST00000438658
  gene symbol: RNH1
  hgvsc: ENST00000438658.2:c.-19-27G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000533592
  gene symbol: RNH1
  hgvsc: ENST00000533592.1:n.976G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380738
  ensembl transcript: ENST00000397614
  gene symbol: RNH1
  hgvsc: ENST00000397614.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-46G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000431201
  ensembl transcript: ENST00000524464
  gene symbol: RNH1
  hgvsc: ENST00000524464.1:c.-19-27G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433033
  ensembl transcript: ENST00000529115
  gene symbol: RNH1
  hgvsc: ENST00000529115.1:c.-19-27G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-46G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.298G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.142G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-19-27G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-19-27G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435798
  ensembl transcript: ENST00000531149
  gene symbol: RNH1
  hgvsc: ENST00000531149.1:c.-19-27G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.8G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435594
  ensembl transcript: ENST00000533410
  gene symbol: RNH1
  hgvsc: ENST00000533410.1:c.-19-27G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000346402
  ensembl transcript: ENST00000354420
  gene symbol: RNH1
  hgvsc: ENST00000354420.2:c.-46G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-19-27G>A
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/10074
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

11-502209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502209
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502209
    reference: chr 11
allele count: 2
allele frequency: 4.211412929037692e-5
allele num: 47490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000533592
  gene symbol: RNH1
  hgvsc: ENST00000533592.1:n.975C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.7C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-47C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.141C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.297C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-47C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-47C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-47C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000431201
  ensembl transcript: ENST00000524464
  gene symbol: RNH1
  hgvsc: ENST00000524464.1:c.-19-28C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-19-28C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380738
  ensembl transcript: ENST00000397614
  gene symbol: RNH1
  hgvsc: ENST00000397614.1:c.-47C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435594
  ensembl transcript: ENST00000533410
  gene symbol: RNH1
  hgvsc: ENST00000533410.1:c.-19-28C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000416589
  ensembl transcript: ENST00000438658
  gene symbol: RNH1
  hgvsc: ENST00000438658.2:c.-19-28C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-47C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-19-28C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-47C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000346402
  ensembl transcript: ENST00000354420
  gene symbol: RNH1
  hgvsc: ENST00000354420.2:c.-47C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433033
  ensembl transcript: ENST00000529115
  gene symbol: RNH1
  hgvsc: ENST00000529115.1:c.-19-28C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-19-28C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000525522
  gene symbol: RNH1
  hgvsc: ENST00000525522.1:n.1059-28C>T
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-47C>T
  variant of: http://identifiers.org/hgnc/10074
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

11-502213-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502213
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502213
    reference: chr 11
allele count: 1
allele frequency: 2.204391147165153e-5
allele num: 45364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000525522
  gene symbol: RNH1
  hgvsc: ENST00000525522.1:n.1059-32A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.293A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.3A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-51A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000431201
  ensembl transcript: ENST00000524464
  gene symbol: RNH1
  hgvsc: ENST00000524464.1:c.-19-32A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380738
  ensembl transcript: ENST00000397614
  gene symbol: RNH1
  hgvsc: ENST00000397614.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-19-32A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-51A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000346402
  ensembl transcript: ENST00000354420
  gene symbol: RNH1
  hgvsc: ENST00000354420.2:c.-51A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435594
  ensembl transcript: ENST00000533410
  gene symbol: RNH1
  hgvsc: ENST00000533410.1:c.-19-32A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-51A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.137A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-19-32A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435798
  ensembl transcript: ENST00000531149
  gene symbol: RNH1
  hgvsc: ENST00000531149.1:c.-19-32A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000533592
  gene symbol: RNH1
  hgvsc: ENST00000533592.1:n.971A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433033
  ensembl transcript: ENST00000529115
  gene symbol: RNH1
  hgvsc: ENST00000529115.1:c.-19-32A>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-19-32A>G
  variant of: http://identifiers.org/hgnc/10074
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum

11-502214-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 502214
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 502214
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 44950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380739
  ensembl transcript: ENST00000397615
  gene symbol: RNH1
  hgvsc: ENST00000397615.2:c.-52C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434971
  ensembl transcript: ENST00000532055
  gene symbol: RNH1
  hgvsc: ENST00000532055.1:c.-52C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000434947
  ensembl transcript: ENST00000529306
  gene symbol: RNH1
  hgvsc: ENST00000529306.1:c.-52C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000433999
  ensembl transcript: ENST00000534797
  gene symbol: RNH1
  hgvsc: ENST00000534797.1:c.-52C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380738
  ensembl transcript: ENST00000397614
  gene symbol: RNH1
  hgvsc: ENST00000397614.1:c.-52C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000524780
  gene symbol: RNH1
  hgvsc: ENST00000524780.1:n.136C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000346402
  ensembl transcript: ENST00000354420
  gene symbol: RNH1
  hgvsc: ENST00000354420.2:c.-52C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435748
  ensembl transcript: ENST00000527485
  gene symbol: RNH1
  hgvsc: ENST00000527485.1:c.-52C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000348515
  ensembl transcript: ENST00000356187
  gene symbol: RNH1
  hgvsc: ENST00000356187.5:c.-52C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000525522
  gene symbol: RNH1
  hgvsc: ENST00000525522.1:n.1059-33C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000432781
  ensembl transcript: ENST00000531540
  gene symbol: RNH1
  hgvsc: ENST00000531540.1:c.-19-33C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000528713
  gene symbol: RNH1
  hgvsc: ENST00000528713.1:n.292C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000380729
  ensembl transcript: ENST00000397604
  gene symbol: RNH1
  hgvsc: ENST00000397604.3:c.-19-33C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000436022
  ensembl transcript: ENST00000525701
  gene symbol: RNH1
  hgvsc: ENST00000525701.1:c.-52C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000526295
  gene symbol: RNH1
  hgvsc: ENST00000526295.1:n.488C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000533592
  gene symbol: RNH1
  hgvsc: ENST00000533592.1:n.970C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435594
  ensembl transcript: ENST00000533410
  gene symbol: RNH1
  hgvsc: ENST00000533410.1:c.-19-33C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000023191
  ensembl transcript: ENST00000531223
  gene symbol: RNH1
  hgvsc: ENST00000531223.1:n.2C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435057
  ensembl transcript: ENST00000529368
  gene symbol: RNH1
  hgvsc: ENST00000529368.1:c.-19-33C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000435798
  ensembl transcript: ENST00000531149
  gene symbol: RNH1
  hgvsc: ENST00000531149.1:c.-19-33C>G
  variant of: http://identifiers.org/hgnc/10074
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000023191
  ensembl protein: ENSP00000416589
  ensembl transcript: ENST00000438658
  gene symbol: RNH1
  hgvsc: ENST00000438658.2:c.-19-33C>G
  variant of: http://identifiers.org/hgnc/10074
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

11-532585-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532585
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532585
    reference: chr 11
allele count: 2
allele frequency: 2.444270629644114e-5
allele num: 81824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*190C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*51C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*190C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*51C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+46C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.288C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+46C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+46C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10146
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19537
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11350
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5712
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5896
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1932
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7997
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-532594-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532594
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532594
    reference: chr 11
allele count: 1
allele frequency: 1.19002284843869e-5
allele num: 84032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+37G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+37G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*181G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*181G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*42G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.279G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+37G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19333
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5168
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7704
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3188
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1907
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6826
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

11-532595-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532595
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532595
    reference: chr 11
allele count: 2
allele frequency: 2.377668933377716e-5
allele num: 84116
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.278C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+36C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+36C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+36C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*41C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*180C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*41C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*180C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5921
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3158
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5028
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3009
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1150
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

11-532596-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532596
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532596
    reference: chr 11
allele count: 284
allele frequency: 3.341097856521023e-3
allele num: 85002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*179C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*40C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+35C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+35C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*40C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.277C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+35C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*179C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 9350
  bin: 2.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14316
  bin: 7.5e0
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18721
  bin: 1.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 1.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15907
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7420
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4814
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.75e1
  variant carriers: 2
num of homozygotes: 1
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

11-532601-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532601
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532601
    reference: chr 11
allele count: 1
allele frequency: 1.178522604063546e-5
allele num: 84852
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*35G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*35G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+30G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*174G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.272G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*174G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+30G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+30G>C
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13852
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14421
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1734
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4421
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5481
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2194
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-532601-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532601
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532601
    reference: chr 11
allele count: 4
allele frequency: 4.714090416254184e-5
allele num: 84852
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*35G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.272G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*174G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+30G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*35G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+30G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+30G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*174G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17958
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13852
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9295
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4421
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3053
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-532602-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532602
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532602
    reference: chr 11
allele count: 31
allele frequency: 3.616678722262408e-4
allele num: 85714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+29C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*34C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*173C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*173C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+29C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.271C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+29C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13748
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17158
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2964
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11209
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5300
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 8.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

11-532606-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532606
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532606
    reference: chr 11
allele count: 3
allele frequency: 3.459010722933241e-5
allele num: 86730
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*169G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+25G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*30G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.267G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*169G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*30G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+25G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+25G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14815
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4929
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3436
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13493
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2782
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

11-532607-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532607
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532607
    reference: chr 11
allele count: 50
allele frequency: 5.654061878053193e-4
allele num: 88432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.266C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+24C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*29C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*29C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*168C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*168C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+24C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+24C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16381
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13206
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14616
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14703
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4694
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15088
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/11-532609-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532609
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532609
    reference: chr 11
allele count: 1
allele frequency: 1.125796501024475e-5
allele num: 88826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+22G>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*166G>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+22G>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*27G>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.264G>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*166G>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*27G>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+22G>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12952
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5053
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14278
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4356
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 712
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

11-532610-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532610
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532610
    reference: chr 11
allele count: 1
allele frequency: 1.103046614749939e-5
allele num: 90658
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*26G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.263G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*165G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+21G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*165G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*26G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+21G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+21G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12740
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2521
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4798
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

11-532611-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532611
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532611
    reference: chr 11
allele count: 9
allele frequency: 9.866906395947991e-5
allele num: 91214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*25C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*164C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+20C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+20C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*25C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*164C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.262C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+20C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11977
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20298
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4394
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18865
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 9.75e1
  variant carriers: 8
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

11-532617-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532617
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532617
    reference: chr 11
allele count: 2
allele frequency: 2.062706270627063e-5
allele num: 96960
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*19C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*19C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*158C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+14C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+14C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*158C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.256C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+14C>G
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2791
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-532620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532620
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532620
    reference: chr 11
allele count: 4
allele frequency: 4.036734281965889e-5
allele num: 99090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*155C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*5+11C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*144+11C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*16C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*155C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.253C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.350+11C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27969
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11149
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

11-532633-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532633
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532633
    reference: chr 11
allele count: 1
allele frequency: 9.226794611551947e-6
allele num: 108380
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*3C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.348C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-3C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*3C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*3C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34304
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3188
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5994
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 7.25e1
  variant carriers: 0
hgvs: c.*3C>T
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

11-532635-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532635
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532635
    reference: chr 11
allele count: 3
allele frequency: 2.727669479196974e-5
allele num: 109984
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*140C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-5C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.*1C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*140C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.*1C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.346C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.*1C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*140C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2049
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3195
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5357
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
hgvs: n.243-5C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff

11-532660-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532660
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532660
    reference: chr 11
allele count: 3
allele frequency: 2.565198802907225e-5
allele num: 116950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.321G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.467G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*115G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.546G>A
  hgvsp: ENSP00000407586.1:p.Met182Ile
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.546G>A
  hgvsp: ENSP00000309845.7:p.Met182Ile
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*115G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*115G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-30G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.546G>A
  hgvsp: ENSP00000380723.2:p.Met182Ile
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2353
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2511
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Met182Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

11-532668-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532668
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532668
    reference: chr 11
allele count: 2
allele frequency: 1.695547492285259e-5
allele num: 117956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*107G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.538G>A
  hgvsp: ENSP00000407586.1:p.Gly180Ser
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.459G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-38G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.538G>A
  hgvsp: ENSP00000380723.2:p.Gly180Ser
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*107G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.313G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*107G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.538G>A
  hgvsp: ENSP00000309845.7:p.Gly180Ser
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2570
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly180Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

11-532669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532669
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532669
    reference: chr 11
allele count: 5
allele frequency: 4.233843652621596e-5
allele num: 118096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*106C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.537C>T
  hgvsp: ENST00000451590.1:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*106C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.537C>T
  hgvsp: ENST00000311189.7:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*106C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.537C>T
  hgvsp: ENST00000397596.2:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-39C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.458C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.312C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11902
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2392
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3233
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Pro179Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-532670-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532670
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532670
    reference: chr 11
allele count: 1
allele frequency: 8.45594452900389e-6
allele num: 118260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-40C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.536C>T
  hgvsp: ENSP00000380723.2:p.Pro179Leu
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.311C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*105C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.536C>T
  hgvsp: ENSP00000407586.1:p.Pro179Leu
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.536C>T
  hgvsp: ENSP00000309845.7:p.Pro179Leu
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*105C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.457C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*105C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39543
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro179Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

11-532672-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532672
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532672
    reference: chr 11
allele count: 3
allele frequency: 2.533869387479307e-5
allele num: 118396
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.534C>G
  hgvsp: ENST00000451590.1:c.534C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.534C>G
  hgvsp: ENST00000397596.2:c.534C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*103C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*103C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-42C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.455C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.534C>G
  hgvsp: ENST00000311189.7:c.534C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*103C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.309C>G
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12062
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly178Gly
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

11-532686-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532686
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532686
    reference: chr 11
allele count: 20
allele frequency: 1.681350460690026e-4
allele num: 118952
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*89C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*89C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*89C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-56C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.520C>T
  hgvsp: ENSP00000407586.1:p.Pro174Ser
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.520C>T
  hgvsp: ENSP00000380723.2:p.Pro174Ser
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.441C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.295C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: uncertain_significance
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.520C>T
  hgvsp: ENSP00000309845.7:p.Pro174Ser
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3248
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 2430
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro174Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/11-532687-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532687
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532687
    reference: chr 11
allele count: 1
allele frequency: 8.405197774303629e-6
allele num: 118974
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.519T>G
  hgvsp: ENST00000311189.7:c.519T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*88T>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.519T>G
  hgvsp: ENST00000397596.2:c.519T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-57T>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.294T>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*88T>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*88T>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.519T>G
  hgvsp: ENST00000451590.1:c.519T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.440T>G
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2431
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7416
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro173Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-532690-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532690
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532690
    reference: chr 11
allele count: 1
allele frequency: 8.399549784131571e-6
allele num: 119054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.291C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*85C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-60C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*85C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.437C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.516C>T
  hgvsp: ENST00000311189.7:c.516C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*85C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.516C>T
  hgvsp: ENST00000451590.1:c.516C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.516C>T
  hgvsp: ENST00000397596.2:c.516C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2612
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn172Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-532696-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532696
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532696
    reference: chr 11
allele count: 3
allele frequency: 2.518384204694268e-5
allele num: 119124
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*79G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-66G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  clinical significance: benign&likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.510G>A
  hgvsp: ENST00000451590.1:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.285G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.510G>A
  hgvsp: ENST00000311189.7:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*79G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.510G>A
  hgvsp: ENST00000397596.2:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*79G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign&likely_benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.431G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12603
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4721
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys170Lys
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

11-532698-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532698
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532698
    reference: chr 11
allele count: 4
allele frequency: 3.356324153786773e-5
allele num: 119178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*77A>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*77A>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.508A>T
  hgvsp: ENSP00000407586.1:p.Lys170Ter
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.429A>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.508A>T
  hgvsp: ENSP00000380723.2:p.Lys170Ter
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.283A>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*77A>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.508A>T
  hgvsp: ENSP00000309845.7:p.Lys170Ter
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-68A>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys170Ter
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

11-532700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532700
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532700
    reference: chr 11
allele count: 3
allele frequency: 2.516736296370866e-5
allele num: 119202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.506G>A
  hgvsp: ENSP00000309845.7:p.Arg169Gln
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.506G>A
  hgvsp: ENSP00000407586.1:p.Arg169Gln
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*75G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*75G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.281G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.427G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-70G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.506G>A
  hgvsp: ENSP00000380723.2:p.Arg169Gln
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*75G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg169Gln
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-532701-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532701
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532701
    reference: chr 11
allele count: 5
allele frequency: 4.193505099302201e-5
allele num: 119232
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.505C>T
  hgvsp: ENSP00000407586.1:p.Arg169Trp
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*74C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.505C>T
  hgvsp: ENSP00000380723.2:p.Arg169Trp
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.426C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*74C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-71C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*74C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.505C>T
  hgvsp: ENSP00000309845.7:p.Arg169Trp
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.280C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg169Trp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

11-532703-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532703
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532703
    reference: chr 11
allele count: 1
allele frequency: 8.38321345338095e-6
allele num: 119286
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.278T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.503T>C
  hgvsp: ENSP00000407586.1:p.Leu168Pro
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*72T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.503T>C
  hgvsp: ENSP00000380723.2:p.Leu168Pro
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*72T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-73T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.503T>C
  hgvsp: ENSP00000309845.7:p.Leu168Pro
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*72T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.424T>C
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40098
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2438
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu168Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD

11-532704-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532704
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532704
    reference: chr 11
allele count: 1
allele frequency: 8.381948635418762e-6
allele num: 119304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.277C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.502C>G
  hgvsp: ENSP00000380723.2:p.Leu168Val
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.502C>G
  hgvsp: ENSP00000407586.1:p.Leu168Val
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-74C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*71C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*71C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*71C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.423C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.502C>G
  hgvsp: ENSP00000309845.7:p.Leu168Val
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7454
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2440
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu168Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS

11-532715-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532715
    reference: chr 11
allele count: 1
allele frequency: 8.373946976167747e-6
allele num: 119418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.491G>A
  hgvsp: ENSP00000380723.2:p.Arg164Gln
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.491G>A
  hgvsp: ENSP00000309845.7:p.Arg164Gln
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.491G>A
  hgvsp: ENSP00000407586.1:p.Arg164Gln
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*60G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*60G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.266G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*60G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.412G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-85G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40091
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2613
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg164Gln
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP

11-532715-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532715
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532715
    reference: chr 11
allele count: 1
allele frequency: 8.373946976167747e-6
allele num: 119418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-85G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.266G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.412G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*60G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*60G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.491G>C
  hgvsp: ENSP00000407586.1:p.Arg164Pro
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.491G>C
  hgvsp: ENSP00000309845.7:p.Arg164Pro
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.491G>C
  hgvsp: ENSP00000380723.2:p.Arg164Pro
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*60G>C
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40091
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3236
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg164Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-532716-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532716
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532716
    reference: chr 11
allele count: 2
allele frequency: 1.674424835069154e-5
allele num: 119444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-86C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.490C>T
  hgvsp: ENSP00000309845.7:p.Arg164Trp
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.411C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*59C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*59C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.490C>T
  hgvsp: ENSP00000380723.2:p.Arg164Trp
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*59C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.265C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.490C>T
  hgvsp: ENSP00000407586.1:p.Arg164Trp
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg164Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

11-532724-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532724
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532724
    reference: chr 11
allele count: 2
allele frequency: 1.674368762976358e-5
allele num: 119448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*51G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*51G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.257G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.482G>A
  hgvsp: ENSP00000407586.1:p.Arg161His
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-94G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*51G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.482G>A
  hgvsp: ENSP00000380723.2:p.Arg161His
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.482G>A
  hgvsp: ENSP00000309845.7:p.Arg161His
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.403G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12865
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7506
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg161His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

11-532725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532725
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532725
    reference: chr 11
allele count: 1
allele frequency: 8.37184381488179e-6
allele num: 119448
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.481C>T
  hgvsp: ENSP00000407586.1:p.Arg161Cys
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.402C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.481C>T
  hgvsp: ENSP00000380723.2:p.Arg161Cys
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.481C>T
  hgvsp: ENSP00000309845.7:p.Arg161Cys
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.256C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-95C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40185
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg161Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

11-532729-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532729
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532729
    reference: chr 11
allele count: 163
allele frequency: 1.364336413552966e-3
allele num: 119472
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.477G>A
  hgvsp: ENST00000451590.1:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-99G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.477G>A
  hgvsp: ENST00000397596.2:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.252G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.477G>A
  hgvsp: ENST00000311189.7:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  clinical significance: benign
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.398G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 37038
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12864
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2603
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu159Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

11-532732-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532732
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532732
    reference: chr 11
allele count: 1
allele frequency: 8.36988181726874e-6
allele num: 119476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*43G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*43G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.474G>C
  hgvsp: ENST00000311189.7:c.474G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-102G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*43G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.395G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.474G>C
  hgvsp: ENST00000451590.1:c.474G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.474G>C
  hgvsp: ENST00000397596.2:c.474G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.249G>C
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr158Thr
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

11-532738-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532738
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532738
    reference: chr 11
allele count: 1
allele frequency: 8.370162046337218e-6
allele num: 119472
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.468C>T
  hgvsp: ENST00000451590.1:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.468C>T
  hgvsp: ENST00000397596.2:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.389C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.468C>T
  hgvsp: ENST00000311189.7:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.243C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-108C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2445
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Phe156Phe
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-532741-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532741
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532741
    reference: chr 11
allele count: 2
allele frequency: 1.674228599172931e-5
allele num: 119458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.386C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.465C>T
  hgvsp: ENST00000397596.2:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.465C>T
  hgvsp: ENST00000311189.7:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*34C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.240C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.465C>T
  hgvsp: ENST00000451590.1:c.465C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-111C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7482
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala155Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP

11-532746-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532746
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532746
    reference: chr 11
allele count: 2
allele frequency: 1.674929652954576e-5
allele num: 119408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.460G>A
  hgvsp: ENSP00000380723.2:p.Asp154Asn
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.460G>A
  hgvsp: ENSP00000407586.1:p.Asp154Asn
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.460G>A
  hgvsp: ENSP00000309845.7:p.Asp154Asn
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.381G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*29G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-116G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.235G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36758
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2605
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp154Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

11-532760-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532760
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532760
    reference: chr 11
allele count: 2
allele frequency: 1.67709259228202e-5
allele num: 119254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-5C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-5C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-5C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-5C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-5C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-130C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-5C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-5C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-5C>G
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7426
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
hgvs: c.451-5C>G
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

11-532760-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532760
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532760
    reference: chr 11
allele count: 2
allele frequency: 1.67709259228202e-5
allele num: 119254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-5C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-5C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-5C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-5C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-5C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-5C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-5C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-130C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-5C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1239
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2583
  bin: 7.75e1
  variant carriers: 0
hgvs: c.451-5C>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

11-532763-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532763
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532763
    reference: chr 11
allele count: 1
allele frequency: 8.387432271484408e-6
allele num: 119226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-8T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-8T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-133T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-8T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-8T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-8T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-8T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-8T>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-8T>C
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2583
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
hgvs: c.451-8T>C
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

11-532764-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532764
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532764
    reference: chr 11
allele count: 1
allele frequency: 8.390247176681825e-6
allele num: 119186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-9C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-9C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-9C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-9C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-9C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-9C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-9C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-9C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-134C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3260
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39304
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

11-532764-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532764
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532764
    reference: chr 11
allele count: 1
allele frequency: 8.390247176681825e-6
allele num: 119186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-9C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-9C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-9C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-9C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-9C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-9C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-9C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-9C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-134C>G
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39304
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

11-532768-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532768
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532768
    reference: chr 11
allele count: 2
allele frequency: 1.678415575696542e-5
allele num: 119160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-13C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-13C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-13C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-138C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-13C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-13C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-13C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-13C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-13C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12826
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

11-532769-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532769
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532769
    reference: chr 11
allele count: 2
allele frequency: 1.6787255115916e-5
allele num: 119138
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-14C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-14C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-14C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-14C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-14C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-139C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-14C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-14C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-14C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39005
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

11-532772-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532772
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532772
    reference: chr 11
allele count: 1
allele frequency: 8.402937667008386e-6
allele num: 119006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-17C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-17C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-17C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-17C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-17C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-17C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-17C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-17C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-142C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7262
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

11-532775-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532775
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532775
    reference: chr 11
allele count: 1
allele frequency: 8.403220113947665e-6
allele num: 119002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-20T>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-20T>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-20T>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-20T>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-145T>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-20T>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-20T>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-20T>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-20T>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38487
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-532786-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532786
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532786
    reference: chr 11
allele count: 1
allele frequency: 8.439958137807636e-6
allele num: 118484
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-31G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-31G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-31G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-31G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-31G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-31G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-31G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-156G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-31G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2226
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-532787-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532787
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532787
    reference: chr 11
allele count: 1
allele frequency: 8.457231778894133e-6
allele num: 118242
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-32G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-32G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-32G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-32G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-32G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-157G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-32G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-32G>C
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-32G>C
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1337
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS

11-532787-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532787
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532787
    reference: chr 11
allele count: 2
allele frequency: 1.691446355778827e-5
allele num: 118242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-32G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-32G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-32G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-32G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-157G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-32G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-32G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-32G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-32G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-532788-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532788
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532788
    reference: chr 11
allele count: 9
allele frequency: 7.634623867530793e-5
allele num: 117884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-33C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-33C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-33C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-33C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-158C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-33C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-33C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-33C>T
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-33C>T
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

11-532788-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532788
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532788
    reference: chr 11
allele count: 1
allele frequency: 8.482915408367548e-6
allele num: 117884
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-33C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-33C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-33C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-33C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-33C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-158C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-33C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-33C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-33C>G
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-532788-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532788
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532788
    reference: chr 11
allele count: 1
allele frequency: 8.482915408367548e-6
allele num: 117884
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-33C>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-33C>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-33C>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-33C>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-33C>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-158C>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-33C>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-33C>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-33C>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

11-532789-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532789
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532788
    reference: chr 11
allele count: 4
allele frequency: 3.421786514739346e-5
allele num: 116898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-160delG
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-35delG
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-35delG
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-35delG
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-35delG
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-35delG
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-35delG
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-35delG
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-35delG
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1848
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: GC
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

11-532791-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532791
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532791
    reference: chr 11
allele count: 2
allele frequency: 1.708613118731526e-5
allele num: 117054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-36G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-36G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-36G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-36G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-36G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-36G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-36G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-161G>A
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-36G>A
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

11-532793-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 532793
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 532793
    reference: chr 11
allele count: 2
allele frequency: 1.704710114045107e-5
allele num: 117322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380722
  ensembl transcript: ENST00000397594
  gene symbol: HRAS
  hgvsc: ENST00000397594.1:c.*20-38C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000462734
  gene symbol: HRAS
  hgvsc: ENST00000462734.1:n.226-38C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000309845
  ensembl transcript: ENST00000311189
  gene symbol: HRAS
  hgvsc: ENST00000311189.7:c.451-38C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000434023
  ensembl transcript: ENST00000493230
  gene symbol: HRAS
  hgvsc: ENST00000493230.1:c.*20-38C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000388246
  ensembl transcript: ENST00000417302
  gene symbol: HRAS
  hgvsc: ENST00000417302.1:c.*20-38C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000380723
  ensembl transcript: ENST00000397596
  gene symbol: HRAS
  hgvsc: ENST00000397596.2:c.451-38C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl protein: ENSP00000407586
  ensembl transcript: ENST00000451590
  gene symbol: HRAS
  hgvsc: ENST00000451590.1:c.451-38C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000479482
  gene symbol: HRAS
  hgvsc: ENST00000479482.1:n.372-38C>G
  variant of: http://identifiers.org/hgnc/5173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000174775
  ensembl transcript: ENST00000478324
  gene symbol: HRAS
  hgvsc: ENST00000478324.1:n.243-163C>G
  variant of: http://identifiers.org/hgnc/5173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4911
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2263
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31850
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1545
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000023191
ensembl transcript: ENST00000525522
gene symbol: RNH1
hgvsc: ENST00000525522.1:n.1062A>G
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 1998
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 102
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2768
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18608
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4186
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5496
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 940
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3914
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 585
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20833
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4556
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7347
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31441
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2882
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1422
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3506
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5772
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2926
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6036
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6860
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.202099737532808e-5
allele num: 12192
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

QD
type: SiteQuality
SIO_000300: 1.002e1

VQSLOD
type: SiteQuality
SIO_000300: 3.33e-1

DP
type: SiteQuality
SIO_000300: 8.68826e5

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000023191
ensembl transcript: ENST00000533592
gene symbol: RNH1
hgvsc: ENST00000533592.1:n.1005C>T
variant of: http://identifiers.org/hgnc/10074

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000023191
ensembl protein: ENSP00000380738
ensembl transcript: ENST00000397614
gene symbol: RNH1
hgvsc: ENST00000397614.1:c.-17C>T
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 5240
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4399
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20810
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2819
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18697
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 585
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1987
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3848
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 941
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 31207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4817
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3535
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1053
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2883
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6939
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 815
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2880
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6778
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.242664029014178e-5
allele num: 12132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5682
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.931e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.27e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 1.189e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

DP
type: SiteQuality
SIO_000300: 8.63088e5

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000023191
ensembl protein: ENSP00000435594
ensembl transcript: ENST00000533410
gene symbol: RNH1
hgvsc: ENST00000533410.1:c.-19-15C>T
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 582
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8411
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1895
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2936
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2926
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17330
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2865
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 21266
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 936
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10046
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1212
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3125
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3475
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25000
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4229
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 661
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.186133945071051e-5
allele num: 31386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5994
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2170
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.892e0

FS
type: SiteQuality
SIO_000300: 2.093e0

MQ
type: SiteQuality
SIO_000300: 4.775e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.06e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.0e0

DP
type: SiteQuality
SIO_000300: 7.66533e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.912e0

QD
type: SiteQuality
SIO_000300: 7.35e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000023191
ensembl protein: ENSP00000435798
ensembl transcript: ENST00000531149
gene symbol: RNH1
hgvsc: ENST00000531149.1:c.-19-17C>T
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 8451
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2930
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 937
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 585
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 21376
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 2831
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2865
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1887
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17284
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3094
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3459
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25668
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10158
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2493
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4329
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.187352584942946e-5
allele num: 31374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4236
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2156
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4452
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: -1.044e0

DP
type: SiteQuality
SIO_000300: 7.65181e5

BaseQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.11e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.451e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.62e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000023191
ensembl transcript: ENST00000533592
gene symbol: RNH1
hgvsc: ENST00000533592.1:n.980T>C
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 65
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 937
bin: 3.75e1
variant carriers: 4

GenotypeDepth
all individuals: 8998
bin: 2.5e0
variant carriers: 3

GenotypeDepth
all individuals: 3054
bin: 1.75e1
variant carriers: 25

GenotypeDepth
all individuals: 23790
bin: 7.5e0
variant carriers: 41

GenotypeDepth
all individuals: 34
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2659
bin: 2.25e1
variant carriers: 4

GenotypeDepth
all individuals: 2599
bin: 2.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1861
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 188
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 32
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 14516
bin: 1.25e1
variant carriers: 51

GenotypeDepth
all individuals: 587
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 102
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 65
bin: 7.75e1
variant carriers: 5

GenotypeDepth
all individuals: 324
bin: 4.75e1
variant carriers: 4

GenotypeDepth
all individuals: 113
bin: 9.75e1
variant carriers: 15

GenotypeDepth
all individuals: 28
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1680
bin: 9.75e1
variant carriers: 129

GenotypeQuality
all individuals: 1373
bin: 6.75e1
variant carriers: 6

GenotypeQuality
all individuals: 5342
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2778
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11592
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 3584
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 662
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4571
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 20220
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1281
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2961
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 110
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

African
type: Population
allele count: 117
allele frequency: 2.083333333333333e-2
allele num: 5616
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27814
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 5.74052812858783e-4
allele num: 3484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10658
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.3586e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.41e-2

QD
type: SiteQuality
SIO_000300: 1.499e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.58e0

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: 5_prime_UTR_variant
ensembl gene: ENSG00000023191
ensembl protein: ENSP00000346402
ensembl transcript: ENST00000354420
gene symbol: RNH1
hgvsc: ENST00000354420.2:c.-44C>A
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 9062
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2724
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13406
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2535
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24880
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2969
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 590
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 935
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1842
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17983
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 791
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11769
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6004
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2867
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5927
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1581
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 498
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1686
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.804885472947264e-5
allele num: 26282
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3192
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.58e-2

DP
type: SiteQuality
SIO_000300: 7.27844e5

VQSLOD
type: SiteQuality
SIO_000300: -3.494e-1

MQ
type: SiteQuality
SIO_000300: 5.671e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 9.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000023191
ensembl transcript: ENST00000525522
gene symbol: RNH1
hgvsc: ENST00000525522.1:n.1059-27G>A
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 940
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26042
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 9181
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12124
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2894
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2793
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2444
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1837
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 596
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2784
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8350
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11509
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2738
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14559
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 666
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6701
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1582
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2845
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3398
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.247193813918683e-4
allele num: 24054
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

QD
type: SiteQuality
SIO_000300: 9.17e0

VQSLOD
type: SiteQuality
SIO_000300: 2.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.82e-2

DP
type: SiteQuality
SIO_000300: 7.20692e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000023191
ensembl protein: ENSP00000435798
ensembl transcript: ENST00000531149
gene symbol: RNH1
hgvsc: ENST00000531149.1:c.-19-28C>T
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 38
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 321
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 60
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1826
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 590
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2787
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 949
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12005
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2454
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26173
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9214
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2853
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6724
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11535
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2889
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8195
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14765
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2738
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1335
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 671
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.302889405513119e-5
allele num: 24088
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.461e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.867e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.79e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.55e-1

QD
type: SiteQuality
SIO_000300: 1.446e1

DP
type: SiteQuality
SIO_000300: 7.19553e5

FS
type: SiteQuality
SIO_000300: 4.14e0

VQSLOD
type: SiteQuality
SIO_000300: -4.424e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000023191
ensembl protein: ENSP00000416589
ensembl transcript: ENST00000438658
gene symbol: RNH1
hgvsc: ENST00000438658.2:c.-19-32A>G
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 2506
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11572
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 26585
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9307
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 591
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2763
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 947
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2739
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1822
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11146
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2770
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2772
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2595
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10343
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6827
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12563
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3154
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.019386106623587e-4
allele num: 4952
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2502
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.78e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.083e0

QD
type: SiteQuality
SIO_000300: 1.638e1

MQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.054e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.17224e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000023191
ensembl protein: ENSP00000433033
ensembl transcript: ENST00000529115
gene symbol: RNH1
hgvsc: ENST00000529115.1:c.-19-33C>G
variant of: http://identifiers.org/hgnc/10074

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000023191
ensembl protein: ENSP00000431201
ensembl transcript: ENST00000524464
gene symbol: RNH1
hgvsc: ENST00000524464.1:c.-19-33C>G
variant of: http://identifiers.org/hgnc/10074

GenotypeDepth
all individuals: 60
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 66
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 595
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 325
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 189
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2525
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2750
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9310
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26589
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 946
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1831
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2710
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11577
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1349
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11055
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6803
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2532
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10794
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2751
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2774
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2458
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 7.17564e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.83e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

GenotypeQuality
all individuals: 2556
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3177
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4662
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.244467387888854e-5
allele num: 44554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3206
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.588310038119441e-4
allele num: 6296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13988
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5790
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.16086e5

VQSLOD
type: SiteQuality
SIO_000300: 2.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 6009
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15458
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1820
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1222
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1832
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45752
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.967359050445104e-4
allele num: 3370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14136
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.164e0

DP
type: SiteQuality
SIO_000300: 9.52908e5

MQ
type: SiteQuality
SIO_000300: 5.733e1

QD
type: SiteQuality
SIO_000300: 1.184e1

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.401e0

GenotypeQuality
all individuals: 15475
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7530
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1354
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7299
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7708
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.181786446742593e-5
allele num: 45834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3334
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.540832049306626e-4
allele num: 6490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6016
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

QD
type: SiteQuality
SIO_000300: 1.544e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 9.60372e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: -4.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2077
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1600
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1482
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1008
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 967
bin: 1.75e1
variant carriers: 3

GenotypeQuality
all individuals: 497
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 3038
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 5840
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 538
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3248
bin: 9.75e1
variant carriers: 275

GenotypeQuality
all individuals: 8447
bin: 6.25e1
variant carriers: 6

European (Non-Finnish)
type: Population
allele count: 173
allele frequency: 3.733114669198567e-3
allele num: 46342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 8.751458576429405e-4
allele num: 3428
num of homozygotes: 0

South Asian
type: Population
allele count: 78
allele frequency: 5.503033723719486e-3
allele num: 14174
num of homozygotes: 1

African
type: Population
allele count: 3
allele frequency: 4.589963280293758e-4
allele num: 6536
num of homozygotes: 0

Other
type: Population
allele count: 5
allele frequency: 8.169934640522876e-3
allele num: 612
num of homozygotes: 0

Latino
type: Population
allele count: 22
allele frequency: 2.818344862925954e-3
allele num: 7806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6104
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

DP
type: SiteQuality
SIO_000300: 9.6867e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.128e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

QD
type: SiteQuality
SIO_000300: 1.267e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

GenotypeQuality
all individuals: 523
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3053
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6973
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1419
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9295
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 914
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.165533370869245e-5
allele num: 46178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 9.96369e5

BaseQRankSum
type: SiteQuality
SIO_000300: -8.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.687e-1

FS
type: SiteQuality
SIO_000300: 4.143e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

GenotypeQuality
all individuals: 14421
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
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variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5481
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2194
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variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 6973
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1734
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.030371203599551e-5
allele num: 14224
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6126
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.496600112607735e-5
allele num: 46178
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.96369e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 4.143e0

VQSLOD
type: SiteQuality
SIO_000300: -4.687e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

QD
type: SiteQuality
SIO_000300: 8.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

GenotypeQuality
all individuals: 555
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6642
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4033
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1228
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1099
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3063
bin: 9.75e1
variant carriers: 27

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3458
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.141786249732277e-5
allele num: 46690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6186
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.525252525252525e-4
allele num: 7920
num of homozygotes: 0

African
type: Population
allele count: 28
allele frequency: 4.244996967859308e-3
allele num: 6596
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

FS
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 1.012594e6

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.144e1

GenotypeQuality
all individuals: 907
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14508
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2614
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 4.25e1
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
all individuals: 792
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6240
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8008
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.491201908738443e-4
allele num: 6706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.223151315511635e-5
allele num: 47358
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

DP
type: SiteQuality
SIO_000300: 1.045031e6

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

FS
type: SiteQuality
SIO_000300: 3.051e0

QD
type: SiteQuality
SIO_000300: 1.344e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 47

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3680
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.449695563931574e-4
allele num: 6898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.585791309863622e-4
allele num: 6306
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.934812760055478e-5
allele num: 14420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 9.730043060616098e-4
allele num: 48304
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.064734e6

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

QD
type: SiteQuality
SIO_000300: 1.396e1

GenotypeQuality
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variant carriers: 0

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

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: 48674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14454
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.437607820586544e-4
allele num: 6956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.104e1

VQSLOD
type: SiteQuality
SIO_000300: -7.085e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.002e0

DP
type: SiteQuality
SIO_000300: 1.082503e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.9e-3

MQ
type: SiteQuality
SIO_000300: 5.747e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49522
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.18595825426945e-4
allele num: 8432
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.69e0

VQSLOD
type: SiteQuality
SIO_000300: -7.75e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 8.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

DP
type: SiteQuality
SIO_000300: 1.09923e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 402
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.175364362952515e-4
allele num: 8508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7162
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.538461538461538e-3
allele num: 650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.403255552882688e-4
allele num: 49884
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

DP
type: SiteQuality
SIO_000300: 1.117734e6

FS
type: SiteQuality
SIO_000300: 2.432e0

QD
type: SiteQuality
SIO_000300: 1.397e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7054
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52938
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.169668040789759e-4
allele num: 9218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.681e1

DP
type: SiteQuality
SIO_000300: 1.204913e6

VQSLOD
type: SiteQuality
SIO_000300: 8.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7956
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 8.703220191470844e-4
allele num: 4596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9496
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.425e1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.236048e6

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.429e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.582e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7990
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.453582907922102e-5
allele num: 10578
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5366
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59136
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.173e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.719e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.368794e6

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5522
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 5.000666755567409e-5
allele num: 59992
num of homozygotes: 0

African
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East 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: 786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10718
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.678e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

Latino
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allele frequency: 2.645036148827367e-4
allele num: 11342
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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SIO_000300: 1.61e0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64444
num of homozygotes: 0

Latino
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allele frequency: 8.758101243650377e-5
allele num: 11418
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.082725060827251e-5
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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DP
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BaseQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.941e1

FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
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allele frequency: 1.17096018735363e-4
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.199435851337528e-5
allele num: 64522
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6292
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 1.504222e6

MQ
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BaseQRankSum
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VQSLOD
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FS
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QD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

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

European (Finnish)
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allele frequency: 0.0e0
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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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.547508511296812e-5
allele num: 64620
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

FS
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -5.46e-1

BaseQRankSum
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VQSLOD
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MQ
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MQRankSum
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DP
type: SiteQuality
SIO_000300: 1.505118e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

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

East Asian
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allele 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

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.638075507869268e-5
allele num: 64682
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.42e0

VQSLOD
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ClippingRankSum
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MQRankSum
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MQ
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DP
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.91e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Other
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Latino
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East Asian
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South Asian
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European (Finnish)
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MQ
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ClippingRankSum
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ReadPosRankSum
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QD
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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African
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VQSLOD
type: SiteQuality
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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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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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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Latino
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European (Non-Finnish)
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QD
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InbreedingCoeff
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DP
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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African
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allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65108
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.329916123019571e-4
allele num: 8584
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.51896e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.343e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.323e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

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: 8.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40001
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.141185862990143e-5
allele num: 65134
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.238e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

FS
type: SiteQuality
SIO_000300: 5.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

DP
type: SiteQuality
SIO_000300: 1.519747e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.830908375933936e-5
allele num: 10172
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.069650366823219e-5
allele num: 65154
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.213e1

MQ
type: SiteQuality
SIO_000300: 5.904e1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 3.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.52e-1

DP
type: SiteQuality
SIO_000300: 1.520761e6

GenotypeQuality
all individuals: 956
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.672477289467223e-5
allele num: 65168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.59e-1

DP
type: SiteQuality
SIO_000300: 1.521311e6

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.312e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 1586
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533836431682925e-5
allele num: 65196
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.19e0

FS
type: SiteQuality
SIO_000300: 1.229e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

DP
type: SiteQuality
SIO_000300: 1.521697e6

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

QD
type: SiteQuality
SIO_000300: 1.297e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3235
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.815469179426777e-5
allele num: 10188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-1

QD
type: SiteQuality
SIO_000300: 2.625e1

MQRankSum
type: SiteQuality
SIO_000300: -2.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.397e0

DP
type: SiteQuality
SIO_000300: 1.521968e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.931e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532144389287247e-5
allele num: 65268
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.86e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.105e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

QD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.682062858135092e-5
allele num: 11518
num of homozygotes: 0

South Asian
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
allele num: 10202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65268
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6472
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Other
type: Population
allele count: 0
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allele num: 870
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.73e-1

FS
type: SiteQuality
SIO_000300: 3.105e0

DP
type: SiteQuality
SIO_000300: 1.524064e6

MQRankSum
type: SiteQuality
SIO_000300: 1.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.085e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2445
bin: 7.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531768886710373e-5
allele num: 65284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.800078400627205e-5
allele num: 10204
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e0

FS
type: SiteQuality
SIO_000300: 1.606e0

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

DP
type: SiteQuality
SIO_000300: 1.52444e6

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40211
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531768886710373e-5
allele num: 65284
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.152e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 1.524525e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.222e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.396e0

MQRankSum
type: SiteQuality
SIO_000300: -3.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.86e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeQuality
all individuals: 889
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531862745098039e-5
allele num: 65280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

DP
type: SiteQuality
SIO_000300: 1.524538e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.009e0

GenotypeQuality
all individuals: 40147
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 161

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.149425287356322e-3
allele num: 870
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.917727717923604e-4
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 140
allele frequency: 2.144082332761578e-3
allele num: 65296
num of homozygotes: 0

Latino
type: Population
allele count: 18
allele frequency: 1.562771314464317e-3
allele num: 11518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.587e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 1.531457e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.69e-1

GenotypeQuality
all individuals: 40189
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 805
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.541782300339192e-4
allele num: 6486
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65302
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.143999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.028e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.622e0

FS
type: SiteQuality
SIO_000300: 3.561e0

DP
type: SiteQuality
SIO_000300: 1.526198e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-1

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

GenotypeQuality
all individuals: 809
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variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.525578e6

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.771e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.142e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.169e0

QD
type: SiteQuality
SIO_000300: 1.292e1

GenotypeQuality
all individuals: 202
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 2438
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
all individuals: 805
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 2609
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GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.063068582105553e-5
allele num: 65294
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.13e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.26e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 1.525139e6

GenotypeQuality
all individuals: 805
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 50
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 103
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variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532097441397273e-5
allele num: 65270
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.077e0

FS
type: SiteQuality
SIO_000300: 1.24e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.54e-1

QD
type: SiteQuality
SIO_000300: 1.532e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: -1.53e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

DP
type: SiteQuality
SIO_000300: 1.523883e6

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39583
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variant carriers: 0

GenotypeQuality
all individuals: 272
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GenotypeQuality
all individuals: 67
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 808
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GenotypeQuality
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GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 84
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3262
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.069085105729982e-5
allele num: 65166
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

MQ
type: SiteQuality
SIO_000300: 5.918e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

DP
type: SiteQuality
SIO_000300: 1.519411e6

FS
type: SiteQuality
SIO_000300: 9.72e-1

QD
type: SiteQuality
SIO_000300: 1.059e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 272
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variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
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GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 1577
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GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.963093835885355e-4
allele num: 10188
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65166
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.42e-1

DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.918e1

QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.37e-1

FS
type: SiteQuality
SIO_000300: 9.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.535060788407221e-5
allele num: 65144
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.545e0

BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.64e-1

ClippingRankSum
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SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.518169e6

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.535673700052213e-5
allele num: 65118
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6450
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

QD
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MQRankSum
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SIO_000300: -8.44e-1

InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -2.533e0

FS
type: SiteQuality
SIO_000300: 8.03e-1

ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.298e0

DP
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SIO_000300: 1.516564e6

VQSLOD
type: SiteQuality
SIO_000300: -7.998e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 16496
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VQSLOD
type: SiteQuality
SIO_000300: -7.998e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

QD
type: SiteQuality
SIO_000300: 7.86e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

DP
type: SiteQuality
SIO_000300: 1.516564e6

FS
type: SiteQuality
SIO_000300: 8.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.44e-1

BaseQRankSum
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SIO_000300: -2.533e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.298e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10176
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.691117677733357e-5
allele num: 11506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.536192700012289e-5
allele num: 65096
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.446e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.514651e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

FS
type: SiteQuality
SIO_000300: 2.341e0

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.93e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6454
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Latino
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allele frequency: 0.0e0
allele num: 11506
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Other
type: Population
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European (Non-Finnish)
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allele count: 2
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allele num: 65082
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East Asian
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African
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MQRankSum
type: SiteQuality
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DP
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FS
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.884e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8552
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Latino
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European (Finnish)
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African
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Other
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South Asian
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European (Non-Finnish)
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ReadPosRankSum
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DP
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MQ
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VQSLOD
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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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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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Latino
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South Asian
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Other
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European (Non-Finnish)
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allele count: 1
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allele num: 64612
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East Asian
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African
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.486542e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.034e0

GenotypeQuality
all individuals: 1078
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2345
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551686683424883e-5
allele num: 64446
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.334e1

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

DP
type: SiteQuality
SIO_000300: 1.482684e6

FS
type: SiteQuality
SIO_000300: 6.42e-1

GenotypeQuality
all individuals: 809
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2345
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.98003992015968e-5
allele num: 10020
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551686683424883e-5
allele num: 64446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

FS
type: SiteQuality
SIO_000300: 6.42e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

DP
type: SiteQuality
SIO_000300: 1.482684e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.45e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

GenotypeQuality
all individuals: 6858
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 809
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 9.75e1
variant carriers: 9

Latino
type: Population
allele count: 1
allele frequency: 8.713837574067619e-5
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.090580500420652e-4
allele num: 64186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.068697657482704e-5
allele num: 16478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

DP
type: SiteQuality
SIO_000300: 1.477535e6

FS
type: SiteQuality
SIO_000300: 4.408e0

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
all individuals: 648
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3269
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 587
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6858
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.006036217303823e-4
allele num: 9940
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64186
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

DP
type: SiteQuality
SIO_000300: 1.477535e6

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

FS
type: SiteQuality
SIO_000300: 4.408e0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

GenotypeQuality
all individuals: 3269
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1559
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33653
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6858
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.557972143458075e-5
allele num: 64186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.408e0

MQRankSum
type: SiteQuality
SIO_000300: 2.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

QD
type: SiteQuality
SIO_000300: 1.38e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 1.477535e6

GenotypeQuality
all individuals: 1272
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6307
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3266
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2461
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30484
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1806
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.295247088448222e-5
allele num: 63540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.326e1

MQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

MQ
type: SiteQuality
SIO_000300: 5.787e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-2

DP
type: SiteQuality
SIO_000300: 1.482129e6

GenotypeQuality
all individuals: 1804
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3264
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 807
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31094
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1158
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2461
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6316
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.142776328608693e-5
allele num: 63638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.034e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 7.404e0

VQSLOD
type: SiteQuality
SIO_000300: 9.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.963e0

DP
type: SiteQuality
SIO_000300: 1.47854e6

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1791
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6357
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 807
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.133322888923704e-5
allele num: 63830
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

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