15-51529117-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529117
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529117
    reference: chr 15
allele count: 8
allele frequency: 6.589785831960461e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.235C>T
  hgvsp: ENSP00000391139.2:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.235C>T
  hgvsp: ENSP00000383930.3:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.235C>T
  hgvsp: ENSP00000454004.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.235C>T
  hgvsp: ENSP00000453318.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.235C>T
  hgvsp: ENSP00000454039.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.235C>T
  hgvsp: ENSP00000379683.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.235C>T
  hgvsp: ENSP00000452872.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.235C>T
  hgvsp: ENSP00000452627.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.235C>T
  hgvsp: ENSP00000379685.4:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.235C>T
  hgvsp: ENSP00000260433.2:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.235C>T
  hgvsp: ENSP00000390614.2:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.235C>T
  hgvsp: ENSP00000453280.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41063G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.235C>T
  hgvsp: ENSP00000453149.1:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.235C>T
  hgvsp: ENSP00000384389.2:p.Arg79Trp
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg79Trp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

15-51529122-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529122
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529122
    reference: chr 15
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.230A>G
  hgvsp: ENSP00000453280.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.230A>G
  hgvsp: ENSP00000452872.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.230A>G
  hgvsp: ENSP00000379683.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.230A>G
  hgvsp: ENSP00000452627.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.230A>G
  hgvsp: ENSP00000390614.2:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.230A>G
  hgvsp: ENSP00000383930.3:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.230A>G
  hgvsp: ENSP00000391139.2:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.230A>G
  hgvsp: ENSP00000454004.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.230A>G
  hgvsp: ENSP00000379685.4:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.230A>G
  hgvsp: ENSP00000453149.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.230A>G
  hgvsp: ENSP00000260433.2:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.230A>G
  hgvsp: ENSP00000384389.2:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.230A>G
  hgvsp: ENSP00000453318.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41058T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.230A>G
  hgvsp: ENSP00000454039.1:p.Tyr77Cys
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr77Cys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD

15-51529124-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529124
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529124
    reference: chr 15
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.228C>T
  hgvsp: ENST00000561075.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.228C>T
  hgvsp: ENST00000558328.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.228C>T
  hgvsp: ENST00000396404.4:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.228C>T
  hgvsp: ENST00000559646.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.228C>T
  hgvsp: ENST00000559980.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.228C>T
  hgvsp: ENST00000260433.2:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.228C>T
  hgvsp: ENST00000439712.2:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.228C>T
  hgvsp: ENST00000453807.2:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.228C>T
  hgvsp: ENST00000405913.3:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.228C>T
  hgvsp: ENST00000557934.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41056G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.228C>T
  hgvsp: ENST00000405011.2:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.228C>T
  hgvsp: ENST00000396402.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.228C>T
  hgvsp: ENST00000557858.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.228C>T
  hgvsp: ENST00000559878.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr76Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

15-51529133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529133
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529133
    reference: chr 15
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.219C>T
  hgvsp: ENST00000559646.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.219C>T
  hgvsp: ENST00000561075.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.219C>T
  hgvsp: ENST00000559980.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.219C>T
  hgvsp: ENST00000260433.2:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.219C>T
  hgvsp: ENST00000557858.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.219C>T
  hgvsp: ENST00000559878.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.219C>T
  hgvsp: ENST00000439712.2:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.219C>T
  hgvsp: ENST00000405913.3:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.219C>T
  hgvsp: ENST00000405011.2:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.219C>T
  hgvsp: ENST00000396404.4:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.219C>T
  hgvsp: ENST00000558328.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.219C>T
  hgvsp: ENST00000396402.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.219C>T
  hgvsp: ENST00000557934.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41047G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.219C>T
  hgvsp: ENST00000453807.2:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala73Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP

15-51529141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529141
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529141
    reference: chr 15
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.211G>A
  hgvsp: ENSP00000452627.1:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.211G>A
  hgvsp: ENSP00000379685.4:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.211G>A
  hgvsp: ENSP00000452872.1:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.211G>A
  hgvsp: ENSP00000454004.1:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.211G>A
  hgvsp: ENSP00000379683.1:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.211G>A
  hgvsp: ENSP00000390614.2:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.211G>A
  hgvsp: ENSP00000453149.1:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.211G>A
  hgvsp: ENSP00000453318.1:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.211G>A
  hgvsp: ENSP00000384389.2:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.211G>A
  hgvsp: ENSP00000260433.2:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.211G>A
  hgvsp: ENSP00000453280.1:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41039C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.211G>A
  hgvsp: ENSP00000454039.1:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.211G>A
  hgvsp: ENSP00000391139.2:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.211G>A
  hgvsp: ENSP00000383930.3:p.Gly71Ser
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly71Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

15-51529142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529142
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529142
    reference: chr 15
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.210C>T
  hgvsp: ENST00000396404.4:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.210C>T
  hgvsp: ENST00000405011.2:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.210C>T
  hgvsp: ENST00000559878.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.210C>T
  hgvsp: ENST00000561075.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.210C>T
  hgvsp: ENST00000559980.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41038G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.210C>T
  hgvsp: ENST00000557934.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.210C>T
  hgvsp: ENST00000453807.2:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.210C>T
  hgvsp: ENST00000439712.2:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.210C>T
  hgvsp: ENST00000405913.3:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.210C>T
  hgvsp: ENST00000559646.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.210C>T
  hgvsp: ENST00000557858.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.210C>T
  hgvsp: ENST00000558328.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.210C>T
  hgvsp: ENST00000260433.2:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.210C>T
  hgvsp: ENST00000396402.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile70Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

15-51529152-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529152
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529152
    reference: chr 15
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.200G>A
  hgvsp: ENSP00000453318.1:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.200G>A
  hgvsp: ENSP00000453280.1:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.200G>A
  hgvsp: ENSP00000452872.1:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.200G>A
  hgvsp: ENSP00000379683.1:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.200G>A
  hgvsp: ENSP00000391139.2:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.200G>A
  hgvsp: ENSP00000379685.4:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.200G>A
  hgvsp: ENSP00000454039.1:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.200G>A
  hgvsp: ENSP00000383930.3:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.200G>A
  hgvsp: ENSP00000390614.2:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.200G>A
  hgvsp: ENSP00000260433.2:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.200G>A
  hgvsp: ENSP00000384389.2:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41028C>T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.200G>A
  hgvsp: ENSP00000452627.1:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.200G>A
  hgvsp: ENSP00000453149.1:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.200G>A
  hgvsp: ENSP00000454004.1:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Trp67Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

15-51529163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529163
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529163
    reference: chr 15
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.189C>T
  hgvsp: ENST00000559980.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.189C>T
  hgvsp: ENST00000405011.2:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.189C>T
  hgvsp: ENST00000559646.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.189C>T
  hgvsp: ENST00000453807.2:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.189C>T
  hgvsp: ENST00000405913.3:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41017G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.189C>T
  hgvsp: ENST00000558328.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.189C>T
  hgvsp: ENST00000396404.4:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.189C>T
  hgvsp: ENST00000260433.2:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.189C>T
  hgvsp: ENST00000557934.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.189C>T
  hgvsp: ENST00000396402.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.189C>T
  hgvsp: ENST00000557858.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.189C>T
  hgvsp: ENST00000439712.2:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.189C>T
  hgvsp: ENST00000559878.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.189C>T
  hgvsp: ENST00000561075.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly63Gly
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-51529165-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529165
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529165
    reference: chr 15
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.187G>A
  hgvsp: ENSP00000452872.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.187G>A
  hgvsp: ENSP00000391139.2:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.187G>A
  hgvsp: ENSP00000454004.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.187G>A
  hgvsp: ENSP00000453149.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.187G>A
  hgvsp: ENSP00000379683.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.187G>A
  hgvsp: ENSP00000383930.3:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.187G>A
  hgvsp: ENSP00000260433.2:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.187G>A
  hgvsp: ENSP00000454039.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.187G>A
  hgvsp: ENSP00000384389.2:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.187G>A
  hgvsp: ENSP00000379685.4:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.187G>A
  hgvsp: ENSP00000453318.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.187G>A
  hgvsp: ENSP00000390614.2:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.187G>A
  hgvsp: ENSP00000452627.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.187G>A
  hgvsp: ENSP00000453280.1:p.Gly63Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41015C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly63Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

15-51529166-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529166
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529166
    reference: chr 15
allele count: 1147
allele frequency: 9.45137526986272e-3
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.186C>T
  hgvsp: ENST00000439712.2:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41014G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.186C>T
  hgvsp: ENST00000559878.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.186C>T
  hgvsp: ENST00000557934.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.186C>T
  hgvsp: ENST00000405011.2:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.186C>T
  hgvsp: ENST00000405913.3:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.186C>T
  hgvsp: ENST00000453807.2:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.186C>T
  hgvsp: ENST00000260433.2:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.186C>T
  hgvsp: ENST00000396402.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.186C>T
  hgvsp: ENST00000559980.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.186C>T
  hgvsp: ENST00000558328.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.186C>T
  hgvsp: ENST00000396404.4:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.186C>T
  hgvsp: ENST00000557858.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.186C>T
  hgvsp: ENST00000561075.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.186C>T
  hgvsp: ENST00000559646.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 5.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 7657
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 4.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 8.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 5.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 92
genotype quality: GenotypeQuality
hgvs: p.His62His
num of homozygotes: 51
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

15-51529167-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529167
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529167
    reference: chr 15
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.185A>G
  hgvsp: ENSP00000384389.2:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.185A>G
  hgvsp: ENSP00000454004.1:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.185A>G
  hgvsp: ENSP00000453318.1:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.185A>G
  hgvsp: ENSP00000383930.3:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.185A>G
  hgvsp: ENSP00000452872.1:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.185A>G
  hgvsp: ENSP00000454039.1:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.185A>G
  hgvsp: ENSP00000391139.2:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.185A>G
  hgvsp: ENSP00000260433.2:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.185A>G
  hgvsp: ENSP00000453280.1:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.185A>G
  hgvsp: ENSP00000453149.1:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.185A>G
  hgvsp: ENSP00000390614.2:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.185A>G
  hgvsp: ENSP00000379685.4:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.185A>G
  hgvsp: ENSP00000452627.1:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.185A>G
  hgvsp: ENSP00000379683.1:p.His62Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41013T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His62Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

15-51529169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529169
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529169
    reference: chr 15
allele count: 3
allele frequency: 2.472187886279357e-5
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.183C>T
  hgvsp: ENST00000405011.2:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.183C>T
  hgvsp: ENST00000557858.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.183C>T
  hgvsp: ENST00000558328.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.183C>T
  hgvsp: ENST00000559878.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.183C>T
  hgvsp: ENST00000557934.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.183C>T
  hgvsp: ENST00000396404.4:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.183C>T
  hgvsp: ENST00000260433.2:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.183C>T
  hgvsp: ENST00000396402.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.183C>T
  hgvsp: ENST00000439712.2:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.183C>T
  hgvsp: ENST00000453807.2:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.183C>T
  hgvsp: ENST00000559980.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.183C>T
  hgvsp: ENST00000405913.3:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-41011G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.183C>T
  hgvsp: ENST00000561075.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.183C>T
  hgvsp: ENST00000559646.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12310
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser61Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

15-51529191-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529191
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529191
    reference: chr 15
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.161T>C
  hgvsp: ENSP00000379685.4:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.161T>C
  hgvsp: ENSP00000452872.1:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40989A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.161T>C
  hgvsp: ENSP00000454039.1:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.161T>C
  hgvsp: ENSP00000452627.1:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.161T>C
  hgvsp: ENSP00000260433.2:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.161T>C
  hgvsp: ENSP00000453149.1:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.161T>C
  hgvsp: ENSP00000384389.2:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.161T>C
  hgvsp: ENSP00000453318.1:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.161T>C
  hgvsp: ENSP00000453280.1:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.161T>C
  hgvsp: ENSP00000390614.2:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.161T>C
  hgvsp: ENSP00000391139.2:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.161T>C
  hgvsp: ENSP00000383930.3:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.161T>C
  hgvsp: ENSP00000379683.1:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.161T>C
  hgvsp: ENSP00000454004.1:p.Met54Thr
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met54Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

15-51529192-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529192
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529192
    reference: chr 15
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.160A>G
  hgvsp: ENSP00000379685.4:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.160A>G
  hgvsp: ENSP00000383930.3:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.160A>G
  hgvsp: ENSP00000260433.2:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.160A>G
  hgvsp: ENSP00000454004.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.160A>G
  hgvsp: ENSP00000452872.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.160A>G
  hgvsp: ENSP00000384389.2:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40988T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.160A>G
  hgvsp: ENSP00000379683.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.160A>G
  hgvsp: ENSP00000390614.2:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.160A>G
  hgvsp: ENSP00000453318.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.160A>G
  hgvsp: ENSP00000452627.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.160A>G
  hgvsp: ENSP00000453280.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.160A>G
  hgvsp: ENSP00000454039.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.160A>G
  hgvsp: ENSP00000453149.1:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.160A>G
  hgvsp: ENSP00000391139.2:p.Met54Val
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met54Val
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

15-51529199-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529199
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529199
    reference: chr 15
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.153C>T
  hgvsp: ENST00000405913.3:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.153C>T
  hgvsp: ENST00000439712.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.153C>T
  hgvsp: ENST00000396404.4:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.153C>T
  hgvsp: ENST00000559646.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.153C>T
  hgvsp: ENST00000557858.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.153C>T
  hgvsp: ENST00000260433.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.153C>T
  hgvsp: ENST00000405011.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40981G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.153C>T
  hgvsp: ENST00000559878.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.153C>T
  hgvsp: ENST00000559980.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.153C>T
  hgvsp: ENST00000453807.2:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.153C>T
  hgvsp: ENST00000561075.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.153C>T
  hgvsp: ENST00000558328.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.153C>T
  hgvsp: ENST00000396402.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.153C>T
  hgvsp: ENST00000557934.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly51Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS

15-51529206-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529206
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529206
    reference: chr 15
allele count: 1
allele frequency: 8.269793751343841e-6
allele num: 120922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.146G>A
  hgvsp: ENSP00000454004.1:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.146G>A
  hgvsp: ENSP00000383930.3:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.146G>A
  hgvsp: ENSP00000379683.1:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.146G>A
  hgvsp: ENSP00000452627.1:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.146G>A
  hgvsp: ENSP00000384389.2:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.146G>A
  hgvsp: ENSP00000391139.2:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.146G>A
  hgvsp: ENSP00000453149.1:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.146G>A
  hgvsp: ENSP00000390614.2:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40974C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.146G>A
  hgvsp: ENSP00000453318.1:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.146G>A
  hgvsp: ENSP00000452872.1:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.146G>A
  hgvsp: ENSP00000379685.4:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.146G>A
  hgvsp: ENSP00000454039.1:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.146G>A
  hgvsp: ENSP00000260433.2:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.146G>A
  hgvsp: ENSP00000453280.1:p.Gly49Asp
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly49Asp
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

15-51529220-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529220
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529218
    reference: chr 15
allele count: 1
allele frequency: 8.331111703545721e-6
allele num: 120032
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40957_195-40956delAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.146-16_146-15delCT
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11248
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: CAG
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

15-51529226-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529226
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529226
    reference: chr 15
allele count: 1
allele frequency: 8.363161944267889e-6
allele num: 119572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40954A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.146-20T>C
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

15-51529227-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529227
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529227
    reference: chr 15
allele count: 3
allele frequency: 2.508822693137534e-5
allele num: 119578
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40953T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.146-21A>T
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/15-51529232-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529232
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529232
    reference: chr 15
allele count: 1
allele frequency: 8.387291575804341e-6
allele num: 119228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40948A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.146-26T>G
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

15-51529233-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529233
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529233
    reference: chr 15
allele count: 592
allele frequency: 4.967026328595641e-3
allele num: 119186
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40947A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.146-27T>C
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21107
  bin: 2.75e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 2.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 4.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 1.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
num of homozygotes: 26
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

15-51529236-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529236
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529236
    reference: chr 15
allele count: 2
allele frequency: 1.680757012958637e-5
allele num: 118994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40944T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.146-30A>G
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-51529244-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529244
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529244
    reference: chr 15
allele count: 1
allele frequency: 8.437964088024841e-6
allele num: 118512
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40936A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.146-38T>C
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14836
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10539
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-51529255-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51529255
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51529255
    reference: chr 15
allele count: 1
allele frequency: 8.562523546939755e-6
allele num: 116788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-40925T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.146-49A>T
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8360
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

15-51534356-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51534356
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51534356
    reference: chr 15
allele count: 0
allele frequency: NaN
allele num: 0
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35824C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.145+609G>A
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

15-51534928-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51534928
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51534928
    reference: chr 15
allele count: 1
allele frequency: 8.961697704013048e-6
allele num: 111586
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35252T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.145+37A>G
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6221
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10852
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

15-51534939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51534939
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51534939
    reference: chr 15
allele count: 1
allele frequency: 8.796157838256249e-6
allele num: 113686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.145+26C>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35241G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29566
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

15-51534960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51534960
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51534960
    reference: chr 15
allele count: 1
allele frequency: 8.356452852893003e-6
allele num: 119668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35220C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.145+5G>A
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.145+5G>A
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: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS

15-51534972-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51534972
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51534972
    reference: chr 15
allele count: 1
allele frequency: 8.267605866693123e-6
allele num: 120954
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.138A>C
  hgvsp: ENST00000260433.2:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.138A>C
  hgvsp: ENST00000396404.4:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.138A>C
  hgvsp: ENST00000405011.2:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.138A>C
  hgvsp: ENST00000557858.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.138A>C
  hgvsp: ENST00000453807.2:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35208T>G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.138A>C
  hgvsp: ENST00000396402.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.138A>C
  hgvsp: ENST00000559878.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.138A>C
  hgvsp: ENST00000559646.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.138A>C
  hgvsp: ENST00000405913.3:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.138A>C
  hgvsp: ENST00000439712.2:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.138A>C
  hgvsp: ENST00000559980.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.138A>C
  hgvsp: ENST00000557934.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.138A>C
  hgvsp: ENST00000558328.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.138A>C
  hgvsp: ENST00000561075.1:c.138A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser46Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

15-51534978-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51534978
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51534978
    reference: chr 15
allele count: 1
allele frequency: 8.257501940512956e-6
allele num: 121102
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.132A>G
  hgvsp: ENST00000453807.2:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.132A>G
  hgvsp: ENST00000559980.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.132A>G
  hgvsp: ENST00000559646.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.132A>G
  hgvsp: ENST00000260433.2:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.132A>G
  hgvsp: ENST00000439712.2:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.132A>G
  hgvsp: ENST00000405011.2:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.132A>G
  hgvsp: ENST00000557934.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.132A>G
  hgvsp: ENST00000405913.3:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.132A>G
  hgvsp: ENST00000561075.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.132A>G
  hgvsp: ENST00000559878.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.132A>G
  hgvsp: ENST00000396404.4:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.132A>G
  hgvsp: ENST00000557858.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35202T>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.132A>G
  hgvsp: ENST00000396402.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.132A>G
  hgvsp: ENST00000558328.1:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr44Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/15-51534982-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51534982
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51534982
    reference: chr 15
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.128G>T
  hgvsp: ENSP00000453318.1:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.128G>T
  hgvsp: ENSP00000453149.1:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.128G>T
  hgvsp: ENSP00000452627.1:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35198C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.128G>T
  hgvsp: ENSP00000453280.1:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.128G>T
  hgvsp: ENSP00000260433.2:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.128G>T
  hgvsp: ENSP00000452872.1:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.128G>T
  hgvsp: ENSP00000391139.2:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.128G>T
  hgvsp: ENSP00000454004.1:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.128G>T
  hgvsp: ENSP00000384389.2:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.128G>T
  hgvsp: ENSP00000383930.3:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.128G>T
  hgvsp: ENSP00000390614.2:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.128G>T
  hgvsp: ENSP00000454039.1:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.128G>T
  hgvsp: ENSP00000379683.1:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.128G>T
  hgvsp: ENSP00000379685.4:p.Gly43Val
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly43Val
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

15-51534987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51534987
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51534987
    reference: chr 15
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.123T>C
  hgvsp: ENST00000557934.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.123T>C
  hgvsp: ENST00000439712.2:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.123T>C
  hgvsp: ENST00000396404.4:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.123T>C
  hgvsp: ENST00000559646.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.123T>C
  hgvsp: ENST00000453807.2:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.123T>C
  hgvsp: ENST00000396402.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.123T>C
  hgvsp: ENST00000558328.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.123T>C
  hgvsp: ENST00000559980.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.123T>C
  hgvsp: ENST00000557858.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.123T>C
  hgvsp: ENST00000260433.2:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.123T>C
  hgvsp: ENST00000561075.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.123T>C
  hgvsp: ENST00000405011.2:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.123T>C
  hgvsp: ENST00000559878.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35193A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.123T>C
  hgvsp: ENST00000405913.3:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr41Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

15-51534995-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51534995
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51534995
    reference: chr 15
allele count: 397
allele frequency: 3.272823201596017e-3
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.115T>C
  hgvsp: ENSP00000384389.2:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.115T>C
  hgvsp: ENSP00000379685.4:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35185A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.115T>C
  hgvsp: ENSP00000454039.1:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.115T>C
  hgvsp: ENSP00000453280.1:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.115T>C
  hgvsp: ENSP00000390614.2:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.115T>C
  hgvsp: ENSP00000452872.1:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.115T>C
  hgvsp: ENSP00000453318.1:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.115T>C
  hgvsp: ENSP00000453149.1:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.115T>C
  hgvsp: ENSP00000452627.1:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.115T>C
  hgvsp: ENSP00000454004.1:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.115T>C
  hgvsp: ENSP00000379683.1:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.115T>C
  hgvsp: ENSP00000383930.3:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.115T>C
  hgvsp: ENSP00000260433.2:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.115T>C
  hgvsp: ENSP00000391139.2:p.Trp39Arg
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 7.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 8.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 5.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 8.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Trp39Arg
num of homozygotes: 10
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

15-51535001-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535001
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535001
    reference: chr 15
allele count: 205
allele frequency: 1.689579006362707e-3
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.109T>C
  hgvsp: ENST00000439712.2:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.109T>C
  hgvsp: ENST00000559646.1:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.109T>C
  hgvsp: ENST00000396404.4:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.109T>C
  hgvsp: ENST00000559980.1:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.109T>C
  hgvsp: ENST00000558328.1:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.109T>C
  hgvsp: ENST00000405011.2:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.109T>C
  hgvsp: ENST00000557934.1:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.109T>C
  hgvsp: ENST00000559878.1:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.109T>C
  hgvsp: ENST00000453807.2:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.109T>C
  hgvsp: ENST00000557858.1:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.109T>C
  hgvsp: ENST00000396402.1:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.109T>C
  hgvsp: ENST00000405913.3:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.109T>C
  hgvsp: ENST00000561075.1:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.109T>C
  hgvsp: ENST00000260433.2:c.109T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35179A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 34473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu37Leu
num of homozygotes: 2
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

15-51535011-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535011
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535011
    reference: chr 15
allele count: 3
allele frequency: 2.472147142197904e-5
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.99C>A
  hgvsp: ENST00000559878.1:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.99C>A
  hgvsp: ENST00000557934.1:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.99C>A
  hgvsp: ENST00000559980.1:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.99C>A
  hgvsp: ENST00000405011.2:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35169G>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.99C>A
  hgvsp: ENST00000396402.1:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.99C>A
  hgvsp: ENST00000396404.4:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.99C>A
  hgvsp: ENST00000561075.1:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.99C>A
  hgvsp: ENST00000453807.2:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.99C>A
  hgvsp: ENST00000405913.3:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.99C>A
  hgvsp: ENST00000439712.2:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.99C>A
  hgvsp: ENST00000260433.2:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.99C>A
  hgvsp: ENST00000557858.1:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.99C>A
  hgvsp: ENST00000559646.1:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.99C>A
  hgvsp: ENST00000558328.1:c.99C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly33Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

15-51535035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535035
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535035
    reference: chr 15
allele count: 10
allele frequency: 8.237639422047218e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.75C>T
  hgvsp: ENST00000405913.3:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.75C>T
  hgvsp: ENST00000557858.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35145G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.75C>T
  hgvsp: ENST00000396404.4:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.75C>T
  hgvsp: ENST00000559980.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.75C>T
  hgvsp: ENST00000405011.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.75C>T
  hgvsp: ENST00000559646.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.75C>T
  hgvsp: ENST00000439712.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.75C>T
  hgvsp: ENST00000453807.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.75C>T
  hgvsp: ENST00000561075.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.75C>T
  hgvsp: ENST00000396402.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.75C>T
  hgvsp: ENST00000260433.2:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.75C>T
  hgvsp: ENST00000558328.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.75C>T
  hgvsp: ENST00000557934.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.75C>T
  hgvsp: ENST00000559878.1:c.75C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr25Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

15-51535036-G-GAGGCAGCAGGCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535036
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535048
    reference: chr 15
allele count: 43
allele frequency: 3.542068238356481e-4
allele num: 121398
alternate allele: GAGGCAGCAGGCA
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: protein_altering_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: protein altering
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr25delinsMetProAlaAlaSer
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: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

15-51535037-T-TGGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535037
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535040
    reference: chr 15
allele count: 43
allele frequency: 3.542126593956968e-4
allele num: 121396
alternate allele: TGGC
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.70_72dupGCC
  hgvsp: ENSP00000454004.1:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.70_72dupGCC
  hgvsp: ENSP00000452872.1:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.70_72dupGCC
  hgvsp: ENSP00000452627.1:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.70_72dupGCC
  hgvsp: ENSP00000384389.2:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.70_72dupGCC
  hgvsp: ENSP00000379683.1:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.70_72dupGCC
  hgvsp: ENSP00000453318.1:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.70_72dupGCC
  hgvsp: ENSP00000453149.1:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.70_72dupGCC
  hgvsp: ENSP00000390614.2:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.70_72dupGCC
  hgvsp: ENSP00000379685.4:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.70_72dupGCC
  hgvsp: ENSP00000391139.2:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.70_72dupGCC
  hgvsp: ENSP00000383930.3:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.70_72dupGCC
  hgvsp: ENSP00000454039.1:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.70_72dupGCC
  hgvsp: ENSP00000260433.2:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.70_72dupGCC
  hgvsp: ENSP00000453280.1:p.Ala24dup
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35142_195-35140dupGGC
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 9.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala24dup
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/15-51535043-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535043
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535043
    reference: chr 15
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.67G>T
  hgvsp: ENSP00000260433.2:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.67G>T
  hgvsp: ENSP00000452872.1:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35137C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.67G>T
  hgvsp: ENSP00000391139.2:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.67G>T
  hgvsp: ENSP00000379685.4:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.67G>T
  hgvsp: ENSP00000452627.1:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.67G>T
  hgvsp: ENSP00000390614.2:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.67G>T
  hgvsp: ENSP00000453318.1:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.67G>T
  hgvsp: ENSP00000453149.1:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.67G>T
  hgvsp: ENSP00000384389.2:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.67G>T
  hgvsp: ENSP00000454004.1:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.67G>T
  hgvsp: ENSP00000453280.1:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.67G>T
  hgvsp: ENSP00000383930.3:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.67G>T
  hgvsp: ENSP00000454039.1:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.67G>T
  hgvsp: ENSP00000379683.1:p.Ala23Ser
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala23Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

15-51535044-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535044
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535044
    reference: chr 15
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.66T>A
  hgvsp: ENST00000559878.1:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.66T>A
  hgvsp: ENST00000396402.1:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.66T>A
  hgvsp: ENST00000396404.4:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.66T>A
  hgvsp: ENST00000260433.2:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.66T>A
  hgvsp: ENST00000559980.1:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.66T>A
  hgvsp: ENST00000559646.1:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.66T>A
  hgvsp: ENST00000405913.3:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.66T>A
  hgvsp: ENST00000558328.1:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.66T>A
  hgvsp: ENST00000439712.2:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.66T>A
  hgvsp: ENST00000561075.1:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.66T>A
  hgvsp: ENST00000557934.1:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.66T>A
  hgvsp: ENST00000405011.2:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35136A>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.66T>A
  hgvsp: ENST00000557858.1:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.66T>A
  hgvsp: ENST00000453807.2:c.66T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro22Pro
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

15-51535046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535046
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535046
    reference: chr 15
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.64C>T
  hgvsp: ENSP00000379685.4:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.64C>T
  hgvsp: ENSP00000453149.1:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.64C>T
  hgvsp: ENSP00000453318.1:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.64C>T
  hgvsp: ENSP00000453280.1:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.64C>T
  hgvsp: ENSP00000390614.2:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.64C>T
  hgvsp: ENSP00000379683.1:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.64C>T
  hgvsp: ENSP00000383930.3:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.64C>T
  hgvsp: ENSP00000384389.2:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.64C>T
  hgvsp: ENSP00000452627.1:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.64C>T
  hgvsp: ENSP00000452872.1:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.64C>T
  hgvsp: ENSP00000454039.1:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35134G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.64C>T
  hgvsp: ENSP00000454004.1:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.64C>T
  hgvsp: ENSP00000391139.2:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.64C>T
  hgvsp: ENSP00000260433.2:p.Pro22Ser
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro22Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

15-51535046-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535046
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535046
    reference: chr 15
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.64C>A
  hgvsp: ENSP00000452872.1:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.64C>A
  hgvsp: ENSP00000260433.2:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.64C>A
  hgvsp: ENSP00000390614.2:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.64C>A
  hgvsp: ENSP00000453280.1:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.64C>A
  hgvsp: ENSP00000391139.2:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.64C>A
  hgvsp: ENSP00000453318.1:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.64C>A
  hgvsp: ENSP00000454004.1:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.64C>A
  hgvsp: ENSP00000379685.4:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.64C>A
  hgvsp: ENSP00000453149.1:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.64C>A
  hgvsp: ENSP00000383930.3:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.64C>A
  hgvsp: ENSP00000384389.2:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.64C>A
  hgvsp: ENSP00000452627.1:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.64C>A
  hgvsp: ENSP00000454039.1:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.64C>A
  hgvsp: ENSP00000379683.1:p.Pro22Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35134G>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro22Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

15-51535048-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535048
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535048
    reference: chr 15
allele count: 5
allele frequency: 4.11834475487612e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.62T>C
  hgvsp: ENSP00000453280.1:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.62T>C
  hgvsp: ENSP00000452872.1:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.62T>C
  hgvsp: ENSP00000454039.1:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.62T>C
  hgvsp: ENSP00000391139.2:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.62T>C
  hgvsp: ENSP00000454004.1:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.62T>C
  hgvsp: ENSP00000453318.1:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.62T>C
  hgvsp: ENSP00000379685.4:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.62T>C
  hgvsp: ENSP00000384389.2:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.62T>C
  hgvsp: ENSP00000379683.1:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.62T>C
  hgvsp: ENSP00000390614.2:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.62T>C
  hgvsp: ENSP00000453149.1:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.62T>C
  hgvsp: ENSP00000260433.2:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.62T>C
  hgvsp: ENSP00000383930.3:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35132A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.62T>C
  hgvsp: ENSP00000452627.1:p.Met21Thr
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met21Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

15-51535049-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535049
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535049
    reference: chr 15
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.61A>G
  hgvsp: ENSP00000390614.2:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.61A>G
  hgvsp: ENSP00000391139.2:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.61A>G
  hgvsp: ENSP00000453149.1:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.61A>G
  hgvsp: ENSP00000453280.1:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.61A>G
  hgvsp: ENSP00000383930.3:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.61A>G
  hgvsp: ENSP00000454004.1:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.61A>G
  hgvsp: ENSP00000260433.2:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.61A>G
  hgvsp: ENSP00000453318.1:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.61A>G
  hgvsp: ENSP00000379685.4:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.61A>G
  hgvsp: ENSP00000452627.1:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.61A>G
  hgvsp: ENSP00000384389.2:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.61A>G
  hgvsp: ENSP00000452872.1:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.61A>G
  hgvsp: ENSP00000454039.1:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35131T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.61A>G
  hgvsp: ENSP00000379683.1:p.Met21Val
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met21Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

15-51535061-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535061
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535061
    reference: chr 15
allele count: 53
allele frequency: 4.366236633549174e-4
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.49G>A
  hgvsp: ENSP00000390614.2:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.49G>A
  hgvsp: ENSP00000454039.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.49G>A
  hgvsp: ENSP00000391139.2:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35119C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.49G>A
  hgvsp: ENSP00000384389.2:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.49G>A
  hgvsp: ENSP00000452872.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.49G>A
  hgvsp: ENSP00000452627.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.49G>A
  hgvsp: ENSP00000453318.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.49G>A
  hgvsp: ENSP00000454004.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.49G>A
  hgvsp: ENSP00000453280.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.49G>A
  hgvsp: ENSP00000379685.4:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.49G>A
  hgvsp: ENSP00000379683.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.49G>A
  hgvsp: ENSP00000383930.3:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.49G>A
  hgvsp: ENSP00000260433.2:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.49G>A
  hgvsp: ENSP00000453149.1:p.Val17Met
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 9.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val17Met
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

15-51535062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535062
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535062
    reference: chr 15
allele count: 3
allele frequency: 2.471169686985173e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.48C>T
  hgvsp: ENST00000405913.3:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.48C>T
  hgvsp: ENST00000557858.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.48C>T
  hgvsp: ENST00000559980.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.48C>T
  hgvsp: ENST00000453807.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.48C>T
  hgvsp: ENST00000396404.4:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35118G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.48C>T
  hgvsp: ENST00000557934.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.48C>T
  hgvsp: ENST00000558328.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.48C>T
  hgvsp: ENST00000405011.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.48C>T
  hgvsp: ENST00000561075.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.48C>T
  hgvsp: ENST00000559878.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.48C>T
  hgvsp: ENST00000439712.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.48C>T
  hgvsp: ENST00000559646.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.48C>T
  hgvsp: ENST00000396402.1:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.48C>T
  hgvsp: ENST00000260433.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ile16Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

15-51535067-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535067
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535067
    reference: chr 15
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.43A>G
  hgvsp: ENSP00000453318.1:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.43A>G
  hgvsp: ENSP00000390614.2:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.43A>G
  hgvsp: ENSP00000379685.4:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.43A>G
  hgvsp: ENSP00000452872.1:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.43A>G
  hgvsp: ENSP00000383930.3:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.43A>G
  hgvsp: ENSP00000391139.2:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.43A>G
  hgvsp: ENSP00000454004.1:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.43A>G
  hgvsp: ENSP00000454039.1:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.43A>G
  hgvsp: ENSP00000452627.1:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.43A>G
  hgvsp: ENSP00000453280.1:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.43A>G
  hgvsp: ENSP00000260433.2:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.43A>G
  hgvsp: ENSP00000453149.1:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.43A>G
  hgvsp: ENSP00000384389.2:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.43A>G
  hgvsp: ENSP00000379683.1:p.Ser15Gly
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35113T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser15Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff

15-51535068-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535068
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535068
    reference: chr 15
allele count: 205
allele frequency: 1.688521349499209e-3
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.42C>G
  hgvsp: ENST00000405011.2:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.42C>G
  hgvsp: ENST00000557858.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.42C>G
  hgvsp: ENST00000439712.2:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.42C>G
  hgvsp: ENST00000396402.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.42C>G
  hgvsp: ENST00000558328.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.42C>G
  hgvsp: ENST00000405913.3:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.42C>G
  hgvsp: ENST00000559646.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.42C>G
  hgvsp: ENST00000260433.2:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35112G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.42C>G
  hgvsp: ENST00000559878.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.42C>G
  hgvsp: ENST00000396404.4:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.42C>G
  hgvsp: ENST00000559980.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.42C>G
  hgvsp: ENST00000453807.2:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.42C>G
  hgvsp: ENST00000557934.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.42C>G
  hgvsp: ENST00000561075.1:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 9.75e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5166
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr14Thr
num of homozygotes: 2
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

15-51535071-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535071
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535071
    reference: chr 15
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.39C>G
  hgvsp: ENSP00000384389.2:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.39C>G
  hgvsp: ENSP00000453318.1:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.39C>G
  hgvsp: ENSP00000390614.2:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.39C>G
  hgvsp: ENSP00000391139.2:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.39C>G
  hgvsp: ENSP00000454004.1:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.39C>G
  hgvsp: ENSP00000452872.1:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.39C>G
  hgvsp: ENSP00000379685.4:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35109G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.39C>G
  hgvsp: ENSP00000453280.1:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.39C>G
  hgvsp: ENSP00000452627.1:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.39C>G
  hgvsp: ENSP00000383930.3:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.39C>G
  hgvsp: ENSP00000379683.1:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.39C>G
  hgvsp: ENSP00000454039.1:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.39C>G
  hgvsp: ENSP00000453149.1:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.39C>G
  hgvsp: ENSP00000260433.2:p.Ile13Met
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile13Met
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum

15-51535074-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535074
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535074
    reference: chr 15
allele count: 6
allele frequency: 4.941850887885876e-5
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.36C>G
  hgvsp: ENSP00000383930.3:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.36C>G
  hgvsp: ENSP00000390614.2:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.36C>G
  hgvsp: ENSP00000453318.1:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.36C>G
  hgvsp: ENSP00000260433.2:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.36C>G
  hgvsp: ENSP00000379685.4:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.36C>G
  hgvsp: ENSP00000452872.1:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.36C>G
  hgvsp: ENSP00000454004.1:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.36C>G
  hgvsp: ENSP00000384389.2:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.36C>G
  hgvsp: ENSP00000453149.1:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.36C>G
  hgvsp: ENSP00000454039.1:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.36C>G
  hgvsp: ENSP00000379683.1:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.36C>G
  hgvsp: ENSP00000452627.1:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.36C>G
  hgvsp: ENSP00000391139.2:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35106G>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.36C>G
  hgvsp: ENSP00000453280.1:p.Asn12Lys
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn12Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

15-51535076-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535076
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535076
    reference: chr 15
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.34A>C
  hgvsp: ENSP00000452627.1:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.34A>C
  hgvsp: ENSP00000390614.2:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35104T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.34A>C
  hgvsp: ENSP00000383930.3:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.34A>C
  hgvsp: ENSP00000453149.1:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.34A>C
  hgvsp: ENSP00000454004.1:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.34A>C
  hgvsp: ENSP00000453280.1:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.34A>C
  hgvsp: ENSP00000454039.1:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.34A>C
  hgvsp: ENSP00000452872.1:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.34A>C
  hgvsp: ENSP00000379685.4:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.34A>C
  hgvsp: ENSP00000379683.1:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.34A>C
  hgvsp: ENSP00000453318.1:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.34A>C
  hgvsp: ENSP00000384389.2:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.34A>C
  hgvsp: ENSP00000260433.2:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.34A>C
  hgvsp: ENSP00000391139.2:p.Asn12His
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn12His
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

15-51535081-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535081
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535081
    reference: chr 15
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.29A>G
  hgvsp: ENSP00000453318.1:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.29A>G
  hgvsp: ENSP00000379685.4:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.29A>G
  hgvsp: ENSP00000383930.3:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.29A>G
  hgvsp: ENSP00000453280.1:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.29A>G
  hgvsp: ENSP00000454004.1:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.29A>G
  hgvsp: ENSP00000391139.2:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.29A>G
  hgvsp: ENSP00000379683.1:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.29A>G
  hgvsp: ENSP00000452627.1:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.29A>G
  hgvsp: ENSP00000390614.2:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.29A>G
  hgvsp: ENSP00000452872.1:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.29A>G
  hgvsp: ENSP00000384389.2:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.29A>G
  hgvsp: ENSP00000260433.2:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.29A>G
  hgvsp: ENSP00000453149.1:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.29A>G
  hgvsp: ENSP00000454039.1:p.His10Arg
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35099T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His10Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

15-51535086-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535086
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535086
    reference: chr 15
allele count: 6
allele frequency: 4.941850887885876e-5
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.24G>A
  hgvsp: ENST00000559646.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.24G>A
  hgvsp: ENST00000439712.2:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.24G>A
  hgvsp: ENST00000559878.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.24G>A
  hgvsp: ENST00000260433.2:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35094C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.24G>A
  hgvsp: ENST00000557934.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.24G>A
  hgvsp: ENST00000405011.2:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.24G>A
  hgvsp: ENST00000557858.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.24G>A
  hgvsp: ENST00000559980.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.24G>A
  hgvsp: ENST00000405913.3:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.24G>A
  hgvsp: ENST00000561075.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.24G>A
  hgvsp: ENST00000558328.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.24G>A
  hgvsp: ENST00000396404.4:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.24G>A
  hgvsp: ENST00000453807.2:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.24G>A
  hgvsp: ENST00000396402.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro8Pro
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

15-51535087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535087
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535087
    reference: chr 15
allele count: 3
allele frequency: 2.470925443942938e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.23C>T
  hgvsp: ENSP00000379685.4:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.23C>T
  hgvsp: ENSP00000384389.2:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.23C>T
  hgvsp: ENSP00000454004.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.23C>T
  hgvsp: ENSP00000379683.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.23C>T
  hgvsp: ENSP00000453149.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.23C>T
  hgvsp: ENSP00000260433.2:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.23C>T
  hgvsp: ENSP00000390614.2:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.23C>T
  hgvsp: ENSP00000452627.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.23C>T
  hgvsp: ENSP00000454039.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.23C>T
  hgvsp: ENSP00000391139.2:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.23C>T
  hgvsp: ENSP00000453318.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.23C>T
  hgvsp: ENSP00000452872.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.23C>T
  hgvsp: ENSP00000383930.3:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35093G>A
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.23C>T
  hgvsp: ENSP00000453280.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro8Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/15-51535095-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535095
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535095
    reference: chr 15
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.15G>T
  hgvsp: ENSP00000383930.3:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.15G>T
  hgvsp: ENSP00000453318.1:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.15G>T
  hgvsp: ENSP00000453280.1:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.15G>T
  hgvsp: ENSP00000390614.2:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.15G>T
  hgvsp: ENSP00000379683.1:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.15G>T
  hgvsp: ENSP00000452872.1:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.15G>T
  hgvsp: ENSP00000452627.1:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.15G>T
  hgvsp: ENSP00000453149.1:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35085C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.15G>T
  hgvsp: ENSP00000391139.2:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.15G>T
  hgvsp: ENSP00000454004.1:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.15G>T
  hgvsp: ENSP00000379685.4:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.15G>T
  hgvsp: ENSP00000384389.2:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.15G>T
  hgvsp: ENSP00000454039.1:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.15G>T
  hgvsp: ENSP00000260433.2:p.Met5Ile
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met5Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-51535101-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535101
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535100
    reference: chr 15
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.8delT
  hgvsp: ENSP00000453318.1:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.8delT
  hgvsp: ENSP00000379683.1:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.8delT
  hgvsp: ENSP00000260433.2:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35075delA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.8delT
  hgvsp: ENSP00000453149.1:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.8delT
  hgvsp: ENSP00000453280.1:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.8delT
  hgvsp: ENSP00000391139.2:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.8delT
  hgvsp: ENSP00000454004.1:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.8delT
  hgvsp: ENSP00000452627.1:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.8delT
  hgvsp: ENSP00000384389.2:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.8delT
  hgvsp: ENSP00000390614.2:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.8delT
  hgvsp: ENSP00000452872.1:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.8delT
  hgvsp: ENSP00000454039.1:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.8delT
  hgvsp: ENSP00000383930.3:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.8delT
  hgvsp: ENSP00000379685.4:p.Leu3TrpfsTer4
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu3TrpfsTer4
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: CA
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

15-51535108-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535108
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535108
    reference: chr 15
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.2T>C
  hgvsp: ENSP00000390614.2:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.2T>C
  hgvsp: ENSP00000452627.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.2T>C
  hgvsp: ENSP00000453280.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.2T>C
  hgvsp: ENSP00000260433.2:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.2T>C
  hgvsp: ENSP00000454004.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.2T>C
  hgvsp: ENSP00000452872.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.2T>C
  hgvsp: ENSP00000384389.2:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.2T>C
  hgvsp: ENSP00000453318.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.2T>C
  hgvsp: ENSP00000453149.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.2T>C
  hgvsp: ENSP00000379683.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.2T>C
  hgvsp: ENSP00000454039.1:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.2T>C
  hgvsp: ENSP00000379685.4:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35072A>G
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.2T>C
  hgvsp: ENSP00000391139.2:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.2T>C
  hgvsp: ENSP00000383930.3:p.Met1?
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/15-51535118-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535118
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535118
    reference: chr 15
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35062C>A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.-9G>T
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

15-51535119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535119
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535119
    reference: chr 15
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35061C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.-10G>A
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-51535155-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535155
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535155
    reference: chr 15
allele count: 32
allele frequency: 2.63587090822227e-4
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35025A>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.-46T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.-46T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.-38-8T>G
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.-38-8T>G
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

15-51535156-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51535156
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51535156
    reference: chr 15
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259240
  ensembl transcript: ENST00000559909
  gene symbol: RP11-108K3.1
  hgvsc: ENST00000559909.1:n.195-35024A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000383930
  ensembl transcript: ENST00000405913
  gene symbol: CYP19A1
  hgvsc: ENST00000405913.3:c.-47T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453149
  ensembl transcript: ENST00000559878
  gene symbol: CYP19A1
  hgvsc: ENST00000559878.1:c.-47T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.-38-9T>C
  variant of: http://identifiers.org/hgnc/2594
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

15-51606343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51606343
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51606343
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 2
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.-39+4287G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.-39+9670G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.-194+24349G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.-283+23672G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.-39+24349G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl transcript: ENST00000492852
  gene symbol: CYP19A1
  hgvsc: ENST00000492852.1:n.801-962G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.-39+9670G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.-230+24349G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.-39+24349G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.-39+24349G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.-39+24349G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.-39+24291G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.-283+24349G>A
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
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: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

15-51606349-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51606349
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51606349
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 6
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454039
  ensembl transcript: ENST00000561075
  gene symbol: CYP19A1
  hgvsc: ENST00000561075.1:c.-39+24343G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379683
  ensembl transcript: ENST00000396402
  gene symbol: CYP19A1
  hgvsc: ENST00000396402.1:c.-39+24343G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453318
  ensembl transcript: ENST00000559646
  gene symbol: CYP19A1
  hgvsc: ENST00000559646.1:c.-39+4281G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl transcript: ENST00000492852
  gene symbol: CYP19A1
  hgvsc: ENST00000492852.1:n.801-968G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000453280
  ensembl transcript: ENST00000558328
  gene symbol: CYP19A1
  hgvsc: ENST00000558328.1:c.-39+24285G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000454004
  ensembl transcript: ENST00000557934
  gene symbol: CYP19A1
  hgvsc: ENST00000557934.1:c.-39+24343G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452872
  ensembl transcript: ENST00000559980
  gene symbol: CYP19A1
  hgvsc: ENST00000559980.1:c.-283+23666G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000260433
  ensembl transcript: ENST00000260433
  gene symbol: CYP19A1
  hgvsc: ENST00000260433.2:c.-39+9664G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000379685
  ensembl transcript: ENST00000396404
  gene symbol: CYP19A1
  hgvsc: ENST00000396404.4:c.-39+9664G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000390614
  ensembl transcript: ENST00000439712
  gene symbol: CYP19A1
  hgvsc: ENST00000439712.2:c.-283+24343G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000391139
  ensembl transcript: ENST00000453807
  gene symbol: CYP19A1
  hgvsc: ENST00000453807.2:c.-230+24343G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000384389
  ensembl transcript: ENST00000405011
  gene symbol: CYP19A1
  hgvsc: ENST00000405011.2:c.-194+24343G>A
  variant of: http://identifiers.org/hgnc/2594
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137869
  ensembl protein: ENSP00000452627
  ensembl transcript: ENST00000557858
  gene symbol: CYP19A1
  hgvsc: ENST00000557858.1:c.-39+24343G>A
  variant of: http://identifiers.org/hgnc/2594
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

15-51633834-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51633834
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51633834
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 4958
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000186417
  ensembl protein: ENSP00000335196
  ensembl transcript: ENST00000335449
  gene symbol: GLDN
  hgvsc: ENST00000335449.6:c.-48C>T
  variant of: http://identifiers.org/hgnc/29514
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18907
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29446
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5306
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5005
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22199
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 258
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 396
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 3364
  num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

15-51633836-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51633836
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 51633836
    reference: chr 15
allele count: 4
allele frequency: 8.133387555917039e-4
allele num: 4918
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000186417
  ensembl protein: ENSP00000335196
  ensembl transcript: ENST00000335449
  gene symbol: GLDN
  hgvsc: ENST00000335449.6:c.-46A>T
  variant of: http://identifiers.org/hgnc/29514
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18938
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29419
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 12165
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1516
bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 1.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeDepth
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bin: 8.75e1
variant carriers: 1

GenotypeDepth
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bin: 9.75e1
variant carriers: 6

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 368
bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7313
bin: 6.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

South Asian
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allele count: 7
allele frequency: 4.239854633555421e-4
allele num: 16510
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.71e-1

FS
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SIO_000300: 2.569e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

DP
type: SiteQuality
SIO_000300: 2.052383e6

QD
type: SiteQuality
SIO_000300: 1.232e1

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.75e1
variant carriers: 1

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.24e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.896e1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
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SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.45e0

QD
type: SiteQuality
SIO_000300: 1.517e1

GenotypeDepth
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bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 710
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 7685
bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 7.5e0
variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 8.75e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1785
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1944
bin: 7.25e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.91e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.013e0

FS
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SIO_000300: 1.606e0

DP
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
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ReadPosRankSum
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MQ
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SIO_000300: 5.881e1

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
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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

Other
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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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.84e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.983e1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

FS
type: SiteQuality
SIO_000300: 3.377e0

DP
type: SiteQuality
SIO_000300: 2.050957e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
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
allele num: 908
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.18e-1

QD
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DP
type: SiteQuality
SIO_000300: 2.050181e6

MQRankSum
type: SiteQuality
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FS
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

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

Other
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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

African
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allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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FS
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MQ
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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DP
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VQSLOD
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GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
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SIO_000300: -2.7e-1

VQSLOD
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.616e0

InbreedingCoeff
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SIO_000300: -2.0e-4

QD
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DP
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SIO_000300: 2.049081e6

FS
type: SiteQuality
SIO_000300: 3.844e0

ReadPosRankSum
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SIO_000300: 2.09e-1

MQRankSum
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SIO_000300: -7.57e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

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

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

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

Latino
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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: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

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

VQSLOD
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BaseQRankSum
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SIO_000300: -4.639e0

InbreedingCoeff
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FS
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QD
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DP
type: SiteQuality
SIO_000300: 2.048364e6

MQRankSum
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -4.41e-1

ReadPosRankSum
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SIO_000300: 2.0e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

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

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

African
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allele count: 0
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Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

FS
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 11

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1077
allele frequency: 1.035576923076923e-1
allele num: 10400
num of homozygotes: 50

European (Finnish)
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num of homozygotes: 0

Latino
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allele num: 11566
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European (Non-Finnish)
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allele frequency: 3.297263271484668e-4
allele num: 66722
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East Asian
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South Asian
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allele num: 16512
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Other
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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QD
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FS
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 1
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allele num: 10400
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Latino
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
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Other
type: Population
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VQSLOD
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SIO_000300: -3.241e-1

FS
type: SiteQuality
SIO_000300: 6.329e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.76e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.531e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.54e-1

DP
type: SiteQuality
SIO_000300: 2.010018e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.54e-1

QD
type: SiteQuality
SIO_000300: 1.113e1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8638
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 count: 2
allele frequency: 3.02571860816944e-4
allele num: 6610
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: 1.74e-2

DP
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SIO_000300: 2.0098e6

VQSLOD
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SIO_000300: 2.22e0

ReadPosRankSum
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SIO_000300: 9.26e-1

FS
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BaseQRankSum
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SIO_000300: -3.023e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

QD
type: SiteQuality
SIO_000300: 1.504e1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

ReadPosRankSum
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SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: -1.309e0

VQSLOD
type: SiteQuality
SIO_000300: -1.737e-1

ClippingRankSum
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SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.492e1

DP
type: SiteQuality
SIO_000300: 2.005029e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

East Asian
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allele 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: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: -2.32e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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South 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: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66468
num of homozygotes: 0

South Asian
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European (Finnish)
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East Asian
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65954
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European (Finnish)
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allele frequency: 1.535155050660117e-4
allele num: 6514
num of homozygotes: 0

African
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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

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

DP
type: SiteQuality
SIO_000300: 1.954255e6

VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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SIO_000300: 2.783e0

MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 7.8e-3

MQ
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SIO_000300: 5.93e1

QD
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GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65670
num of homozygotes: 0

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

South Asian
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allele frequency: 6.101281269066504e-5
allele num: 16390
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.012e1

DP
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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SIO_000300: 4.65e-1

InbreedingCoeff
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SIO_000300: 5.9e-3

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.567739577940863e-5
allele num: 65678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
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SIO_000300: 5.4e-3

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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DP
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VQSLOD
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MQRankSum
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SIO_000300: 7.099999999999999e-2

ClippingRankSum
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SIO_000300: 1.07e0

ReadPosRankSum
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SIO_000300: 6.12e-1

FS
type: SiteQuality
SIO_000300: 1.073e0

QD
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SIO_000300: 1.309e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.807468733485996e-5
allele num: 11354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65478
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.99e1

VQSLOD
type: SiteQuality
SIO_000300: 2.45e-1

ReadPosRankSum
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SIO_000300: 2.41e0

BaseQRankSum
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SIO_000300: 2.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.118e0

FS
type: SiteQuality
SIO_000300: 3.65e0

MQRankSum
type: SiteQuality
SIO_000300: 7.06e-1

QD
type: SiteQuality
SIO_000300: 1.458e1

DP
type: SiteQuality
SIO_000300: 1.855815e6

GenotypeDepth
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variant carriers: 20

GenotypeDepth
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variant carriers: 11

GenotypeDepth
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variant carriers: 81

GenotypeDepth
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variant carriers: 25

GenotypeDepth
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variant carriers: 64

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 560

South Asian
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allele count: 2
allele frequency: 1.222344456667889e-4
allele num: 16362
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.056234718826406e-5
allele num: 65440
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 1.848266150325647e-3
allele num: 11362
num of homozygotes: 0

African
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allele frequency: 5.485436893203884e-2
allele num: 10300
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Other
type: Population
allele count: 2
allele frequency: 2.262443438914027e-3
allele num: 884
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InbreedingCoeff
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FS
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MQ
type: SiteQuality
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VQSLOD
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DP
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 2
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allele num: 16336
num of homozygotes: 0

East Asian
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allele count: 0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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African
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Other
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European (Non-Finnish)
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QD
type: SiteQuality
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MQ
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ClippingRankSum
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DP
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.536948235583426e-5
allele num: 65064
num of homozygotes: 0

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

Other
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East Asian
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ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -3.0e-4

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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South Asian
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MQ
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InbreedingCoeff
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QD
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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SIO_000300: 1.64e0

DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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Latino
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allele frequency: 0.0e0
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QD
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SIO_000300: 1.331e1

DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -1.205e0

ClippingRankSum
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SIO_000300: 4.71e-1

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 51

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

South Asian
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num of homozygotes: 0

East Asian
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allele num: 8634
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African
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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num of homozygotes: 0

European (Finnish)
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Other
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MQ
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SIO_000300: 5.979e1

ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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allele num: 66704
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East Asian
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African
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Other
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Latino
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African
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East Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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ClippingRankSum
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DP
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MQ
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VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

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

South Asian
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allele count: 10
allele frequency: 6.056201550387597e-4
allele num: 16512
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 1.226e0

BaseQRankSum
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SIO_000300: -4.467e0

ClippingRankSum
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VQSLOD
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QD
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MQRankSum
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SIO_000300: 4.95e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

DP
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SIO_000300: 1.917643e6

ReadPosRankSum
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SIO_000300: 6.54e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 43

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.990919171636647e-5
allele num: 66734
num of homozygotes: 0

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

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

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

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

Latino
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allele count: 34
allele frequency: 2.937111264685557e-3
allele num: 11576
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.46e0

VQSLOD
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SIO_000300: 1.36e0

QD
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SIO_000300: 4.25e0

InbreedingCoeff
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SIO_000300: 2.92e-2

MQRankSum
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SIO_000300: -5.281e0

MQ
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SIO_000300: 5.201e1

ReadPosRankSum
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SIO_000300: 4.5e-2

ClippingRankSum
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SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.81e-1

DP
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SIO_000300: 1.917499e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 43

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 6
allele frequency: 8.990919171636647e-5
allele num: 66734
num of homozygotes: 0

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

Latino
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allele count: 34
allele frequency: 2.938126512270999e-3
allele num: 11572
num of homozygotes: 0

VQSLOD
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SIO_000300: 6.79e-1

MQRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.76e-2

MQ
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SIO_000300: 5.22e1

FS
type: SiteQuality
SIO_000300: 2.392e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

DP
type: SiteQuality
SIO_000300: 1.917641e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: 1.48e-1

MQ
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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FS
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SIO_000300: 5.0e-1

BaseQRankSum
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QD
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SIO_000300: 1.306e1

InbreedingCoeff
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SIO_000300: -1.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

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

Latino
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 5
allele frequency: 7.491983577571999e-5
allele num: 66738
num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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South Asian
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allele frequency: 1.574612403100775e-3
allele num: 16512
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European (Finnish)
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East Asian
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Latino
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allele frequency: 5.191209551825575e-4
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African
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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European (Finnish)
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African
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Latino
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East Asian
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South Asian
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ClippingRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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FS
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SIO_000300: 2.085e0

QD
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InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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Latino
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South Asian
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European (Non-Finnish)
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African
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allele frequency: 1.854699211993081e-2
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European (Finnish)
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East Asian
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 3.633720930232558e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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allele num: 908
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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Latino
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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: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

African
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Other
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InbreedingCoeff
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FS
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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allele num: 66740
num of homozygotes: 0

MQ
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11578
num of homozygotes: 0

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