9-73398999-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73398999
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73398999
    reference: chr 9
allele count: 7
allele frequency: 5.901694629457887e-5
allele num: 118610
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.689+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1148+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.689+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.689+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.764+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.764+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1229+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.*18A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.689+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.764+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.764+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1148+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.689+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1154+22A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.764+22A>G
  variant of: http://identifiers.org/hgnc/17992
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/9-73399009-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399009
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399009
    reference: chr 9
allele count: 1
allele frequency: 8.359107247345984e-6
allele num: 119630
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.764+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.764+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.764+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.764+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.689+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1148+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1229+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.*8T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.689+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.764+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.689+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.689+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.689+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1154+12T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1148+12T>G
  variant of: http://identifiers.org/hgnc/17992
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

9-73399014-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399014
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399014
    reference: chr 9
allele count: 1
allele frequency: 8.337502084375522e-6
allele num: 119940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1229+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1148+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.764+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1154+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.764+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.764+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.689+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.689+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.764+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1148+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.689+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.*3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.689+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.689+7A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.764+7A>G
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1148+7A>G
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-73399018-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399018
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399018
    reference: chr 9
allele count: 2
allele frequency: 1.663312320154355e-5
allele num: 120242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.689+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.764+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.764+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.689+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1154+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.764+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.764+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.692A>G
  hgvsp: ENSP00000355395.4:p.Ter231TrpextTer19
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.689+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1148+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1148+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.764+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.689+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.689+3A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1229+3A>G
  variant of: http://identifiers.org/hgnc/17992
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter231TrpextTer19
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

9-73399022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399022
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399022
    reference: chr 9
allele count: 3
allele frequency: 2.489791853401056e-5
allele num: 120492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.763G>A
  hgvsp: ENSP00000354066.2:p.Gly255Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.763G>A
  hgvsp: ENSP00000366310.1:p.Gly255Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.688G>A
  hgvsp: ENSP00000366309.1:p.Gly230Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.688G>A
  hgvsp: ENSP00000355395.4:p.Gly230Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.688G>A
  hgvsp: ENSP00000386127.2:p.Gly230Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.688G>A
  hgvsp: ENSP00000379576.5:p.Gly230Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1147G>A
  hgvsp: ENSP00000366314.2:p.Gly383Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1147G>A
  hgvsp: ENSP00000366315.2:p.Gly383Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1228G>A
  hgvsp: ENSP00000389542.3:p.Gly410Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1153G>A
  hgvsp: ENSP00000350140.2:p.Gly385Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.688G>A
  hgvsp: ENSP00000366305.1:p.Gly230Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.763G>A
  hgvsp: ENSP00000379587.4:p.Gly255Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.688G>A
  hgvsp: ENSP00000379581.1:p.Gly230Arg
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.763G>A
  hgvsp: ENSP00000379579.1:p.Gly255Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.763G>A
  hgvsp: ENSP00000350791.3:p.Gly255Arg
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly383Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

9-73399023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399023
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399023
    reference: chr 9
allele count: 1
allele frequency: 8.292974192264313e-6
allele num: 120584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.687C>T
  hgvsp: ENST00000377101.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.687C>T
  hgvsp: ENST00000408909.2:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1227C>T
  hgvsp: ENST00000423814.3:c.1227C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.762C>T
  hgvsp: ENST00000358082.3:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1146C>T
  hgvsp: ENST00000377111.2:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.687C>T
  hgvsp: ENST00000377105.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.762C>T
  hgvsp: ENST00000396292.4:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1146C>T
  hgvsp: ENST00000377110.3:c.1146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.762C>T
  hgvsp: ENST00000396283.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.762C>T
  hgvsp: ENST00000377106.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.687C>T
  hgvsp: ENST00000396285.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.687C>T
  hgvsp: ENST00000396280.5:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1152C>T
  hgvsp: ENST00000357533.2:c.1152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.687C>T
  hgvsp: ENST00000361823.5:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.762C>T
  hgvsp: ENST00000360823.2:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1146C>T
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

9-73399062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399062
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399062
    reference: chr 9
allele count: 16
allele frequency: 1.319435281699433e-4
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.723G>A
  hgvsp: ENST00000396292.4:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.648G>A
  hgvsp: ENST00000377101.1:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.723G>A
  hgvsp: ENST00000358082.3:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.648G>A
  hgvsp: ENST00000361823.5:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1113G>A
  hgvsp: ENST00000357533.2:c.1113G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1107G>A
  hgvsp: ENST00000377111.2:c.1107G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.648G>A
  hgvsp: ENST00000377105.1:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.648G>A
  hgvsp: ENST00000396285.1:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.723G>A
  hgvsp: ENST00000360823.2:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.723G>A
  hgvsp: ENST00000396283.1:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.648G>A
  hgvsp: ENST00000396280.5:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.723G>A
  hgvsp: ENST00000377106.1:c.723G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.648G>A
  hgvsp: ENST00000408909.2:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1107G>A
  hgvsp: ENST00000377110.3:c.1107G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1188G>A
  hgvsp: ENST00000423814.3:c.1188G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11243
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15476
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser369Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

9-73399063-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399063
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399063
    reference: chr 9
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.722C>T
  hgvsp: ENSP00000350791.3:p.Ser241Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.722C>T
  hgvsp: ENSP00000379587.4:p.Ser241Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.647C>T
  hgvsp: ENSP00000355395.4:p.Ser216Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1106C>T
  hgvsp: ENSP00000366315.2:p.Ser369Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.647C>T
  hgvsp: ENSP00000366305.1:p.Ser216Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.722C>T
  hgvsp: ENSP00000366310.1:p.Ser241Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1112C>T
  hgvsp: ENSP00000350140.2:p.Ser371Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.647C>T
  hgvsp: ENSP00000379581.1:p.Ser216Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.647C>T
  hgvsp: ENSP00000379576.5:p.Ser216Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.722C>T
  hgvsp: ENSP00000379579.1:p.Ser241Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.647C>T
  hgvsp: ENSP00000366309.1:p.Ser216Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1187C>T
  hgvsp: ENSP00000389542.3:p.Ser396Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.647C>T
  hgvsp: ENSP00000386127.2:p.Ser216Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1106C>T
  hgvsp: ENSP00000366314.2:p.Ser369Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.722C>T
  hgvsp: ENSP00000354066.2:p.Ser241Leu
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser369Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

9-73399065-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399065
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399065
    reference: chr 9
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.645A>G
  hgvsp: ENST00000377101.1:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1185A>G
  hgvsp: ENST00000423814.3:c.1185A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.720A>G
  hgvsp: ENST00000396292.4:c.720A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.720A>G
  hgvsp: ENST00000377106.1:c.720A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1110A>G
  hgvsp: ENST00000357533.2:c.1110A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.645A>G
  hgvsp: ENST00000396280.5:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.645A>G
  hgvsp: ENST00000408909.2:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.720A>G
  hgvsp: ENST00000358082.3:c.720A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.645A>G
  hgvsp: ENST00000377105.1:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.645A>G
  hgvsp: ENST00000361823.5:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.645A>G
  hgvsp: ENST00000396285.1:c.645A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1104A>G
  hgvsp: ENST00000377110.3:c.1104A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1104A>G
  hgvsp: ENST00000377111.2:c.1104A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.720A>G
  hgvsp: ENST00000396283.1:c.720A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.720A>G
  hgvsp: ENST00000360823.2:c.720A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala368Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

9-73399069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399069
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399069
    reference: chr 9
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.641G>A
  hgvsp: ENSP00000366309.1:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.641G>A
  hgvsp: ENSP00000379581.1:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.716G>A
  hgvsp: ENSP00000350791.3:p.Arg239Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.641G>A
  hgvsp: ENSP00000366305.1:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.716G>A
  hgvsp: ENSP00000354066.2:p.Arg239Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.641G>A
  hgvsp: ENSP00000355395.4:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1181G>A
  hgvsp: ENSP00000389542.3:p.Arg394Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.716G>A
  hgvsp: ENSP00000379579.1:p.Arg239Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1106G>A
  hgvsp: ENSP00000350140.2:p.Arg369Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.716G>A
  hgvsp: ENSP00000366310.1:p.Arg239Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.716G>A
  hgvsp: ENSP00000379587.4:p.Arg239Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.641G>A
  hgvsp: ENSP00000386127.2:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.641G>A
  hgvsp: ENSP00000379576.5:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1100G>A
  hgvsp: ENSP00000366315.2:p.Arg367Gln
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1100G>A
  hgvsp: ENSP00000366314.2:p.Arg367Gln
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28698
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg367Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

9-73399071-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399071
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399071
    reference: chr 9
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.639A>G
  hgvsp: ENST00000396280.5:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.639A>G
  hgvsp: ENST00000377105.1:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1098A>G
  hgvsp: ENST00000377111.2:c.1098A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1104A>G
  hgvsp: ENST00000357533.2:c.1104A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.714A>G
  hgvsp: ENST00000377106.1:c.714A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.714A>G
  hgvsp: ENST00000396283.1:c.714A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.714A>G
  hgvsp: ENST00000358082.3:c.714A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.639A>G
  hgvsp: ENST00000361823.5:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.639A>G
  hgvsp: ENST00000377101.1:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1179A>G
  hgvsp: ENST00000423814.3:c.1179A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.714A>G
  hgvsp: ENST00000360823.2:c.714A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.714A>G
  hgvsp: ENST00000396292.4:c.714A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.639A>G
  hgvsp: ENST00000396285.1:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.639A>G
  hgvsp: ENST00000408909.2:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1098A>G
  hgvsp: ENST00000377110.3:c.1098A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11246
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly366Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

9-73399086-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399086
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399086
    reference: chr 9
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.699C>G
  hgvsp: ENST00000396283.1:c.699C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1164C>G
  hgvsp: ENST00000423814.3:c.1164C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.699C>G
  hgvsp: ENST00000360823.2:c.699C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.624C>G
  hgvsp: ENST00000361823.5:c.624C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1083C>G
  hgvsp: ENST00000377111.2:c.1083C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.699C>G
  hgvsp: ENST00000377106.1:c.699C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.624C>G
  hgvsp: ENST00000396285.1:c.624C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1089C>G
  hgvsp: ENST00000357533.2:c.1089C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.624C>G
  hgvsp: ENST00000377101.1:c.624C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.624C>G
  hgvsp: ENST00000408909.2:c.624C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.624C>G
  hgvsp: ENST00000377105.1:c.624C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.624C>G
  hgvsp: ENST00000396280.5:c.624C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.699C>G
  hgvsp: ENST00000396292.4:c.699C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.699C>G
  hgvsp: ENST00000358082.3:c.699C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1083C>G
  hgvsp: ENST00000377110.3:c.1083C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val361Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/9-73399094-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399094
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399094
    reference: chr 9
allele count: 2
allele frequency: 1.649294102124291e-5
allele num: 121264
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.616G>T
  hgvsp: ENSP00000366305.1:p.Val206Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.691G>T
  hgvsp: ENSP00000379587.4:p.Val231Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.616G>T
  hgvsp: ENSP00000366309.1:p.Val206Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.691G>T
  hgvsp: ENSP00000350791.3:p.Val231Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1156G>T
  hgvsp: ENSP00000389542.3:p.Val386Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1075G>T
  hgvsp: ENSP00000366314.2:p.Val359Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.616G>T
  hgvsp: ENSP00000355395.4:p.Val206Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.616G>T
  hgvsp: ENSP00000386127.2:p.Val206Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.691G>T
  hgvsp: ENSP00000366310.1:p.Val231Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.616G>T
  hgvsp: ENSP00000379581.1:p.Val206Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.691G>T
  hgvsp: ENSP00000379579.1:p.Val231Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.691G>T
  hgvsp: ENSP00000354066.2:p.Val231Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1075G>T
  hgvsp: ENSP00000366315.2:p.Val359Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1081G>T
  hgvsp: ENSP00000350140.2:p.Val361Leu
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.616G>T
  hgvsp: ENSP00000379576.5:p.Val206Leu
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val359Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

9-73399100-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399100
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399100
    reference: chr 9
allele count: 14
allele frequency: 1.154639175257732e-4
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.610G>A
  hgvsp: ENSP00000379576.5:p.Val204Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1150G>A
  hgvsp: ENSP00000389542.3:p.Val384Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.610G>A
  hgvsp: ENSP00000379581.1:p.Val204Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.685G>A
  hgvsp: ENSP00000354066.2:p.Val229Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.685G>A
  hgvsp: ENSP00000350791.3:p.Val229Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.685G>A
  hgvsp: ENSP00000366310.1:p.Val229Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.685G>A
  hgvsp: ENSP00000379579.1:p.Val229Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.610G>A
  hgvsp: ENSP00000355395.4:p.Val204Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.610G>A
  hgvsp: ENSP00000386127.2:p.Val204Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1069G>A
  hgvsp: ENSP00000366314.2:p.Val357Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1069G>A
  hgvsp: ENSP00000366315.2:p.Val357Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1075G>A
  hgvsp: ENSP00000350140.2:p.Val359Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.610G>A
  hgvsp: ENSP00000366305.1:p.Val204Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.685G>A
  hgvsp: ENSP00000379587.4:p.Val229Met
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.610G>A
  hgvsp: ENSP00000366309.1:p.Val204Met
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val357Met
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum

9-73399101-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399101
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399101
    reference: chr 9
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.609C>T
  hgvsp: ENST00000377105.1:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.684C>T
  hgvsp: ENST00000360823.2:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1068C>T
  hgvsp: ENST00000377110.3:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.609C>T
  hgvsp: ENST00000377101.1:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.684C>T
  hgvsp: ENST00000377106.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.609C>T
  hgvsp: ENST00000361823.5:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.609C>T
  hgvsp: ENST00000396280.5:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.684C>T
  hgvsp: ENST00000358082.3:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.609C>T
  hgvsp: ENST00000396285.1:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1149C>T
  hgvsp: ENST00000423814.3:c.1149C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.684C>T
  hgvsp: ENST00000396292.4:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.609C>T
  hgvsp: ENST00000408909.2:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.684C>T
  hgvsp: ENST00000396283.1:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1074C>T
  hgvsp: ENST00000357533.2:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1068C>T
  hgvsp: ENST00000377111.2:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro356Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

9-73399106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399106
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399106
    reference: chr 9
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.679C>T
  hgvsp: ENSP00000366310.1:p.Pro227Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1063C>T
  hgvsp: ENSP00000366315.2:p.Pro355Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1144C>T
  hgvsp: ENSP00000389542.3:p.Pro382Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.604C>T
  hgvsp: ENSP00000379576.5:p.Pro202Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.679C>T
  hgvsp: ENSP00000379587.4:p.Pro227Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.679C>T
  hgvsp: ENSP00000379579.1:p.Pro227Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1069C>T
  hgvsp: ENSP00000350140.2:p.Pro357Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.604C>T
  hgvsp: ENSP00000366305.1:p.Pro202Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.604C>T
  hgvsp: ENSP00000355395.4:p.Pro202Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.604C>T
  hgvsp: ENSP00000379581.1:p.Pro202Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.679C>T
  hgvsp: ENSP00000354066.2:p.Pro227Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.604C>T
  hgvsp: ENSP00000386127.2:p.Pro202Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1063C>T
  hgvsp: ENSP00000366314.2:p.Pro355Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.604C>T
  hgvsp: ENSP00000366309.1:p.Pro202Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.679C>T
  hgvsp: ENSP00000350791.3:p.Pro227Ser
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro355Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

9-73399115-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399115
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399115
    reference: chr 9
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.670C>T
  hgvsp: ENSP00000379579.1:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.595C>T
  hgvsp: ENSP00000379581.1:p.Arg199Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.670C>T
  hgvsp: ENSP00000350791.3:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.595C>T
  hgvsp: ENSP00000366305.1:p.Arg199Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.595C>T
  hgvsp: ENSP00000355395.4:p.Arg199Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1054C>T
  hgvsp: ENSP00000366314.2:p.Arg352Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.595C>T
  hgvsp: ENSP00000366309.1:p.Arg199Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.670C>T
  hgvsp: ENSP00000379587.4:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.595C>T
  hgvsp: ENSP00000379576.5:p.Arg199Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.670C>T
  hgvsp: ENSP00000354066.2:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1135C>T
  hgvsp: ENSP00000389542.3:p.Arg379Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.670C>T
  hgvsp: ENSP00000366310.1:p.Arg224Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1060C>T
  hgvsp: ENSP00000350140.2:p.Arg354Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.595C>T
  hgvsp: ENSP00000386127.2:p.Arg199Ter
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1054C>T
  hgvsp: ENSP00000366315.2:p.Arg352Ter
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg352Ter
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum

9-73399126-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399126
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399126
    reference: chr 9
allele count: 3
allele frequency: 2.477291494632535e-5
allele num: 121100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1043T>C
  hgvsp: ENSP00000366315.2:p.Leu348Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.659T>C
  hgvsp: ENSP00000354066.2:p.Leu220Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1124T>C
  hgvsp: ENSP00000389542.3:p.Leu375Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.584T>C
  hgvsp: ENSP00000366305.1:p.Leu195Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.584T>C
  hgvsp: ENSP00000379576.5:p.Leu195Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1049T>C
  hgvsp: ENSP00000350140.2:p.Leu350Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.659T>C
  hgvsp: ENSP00000350791.3:p.Leu220Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.659T>C
  hgvsp: ENSP00000379587.4:p.Leu220Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.584T>C
  hgvsp: ENSP00000355395.4:p.Leu195Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.659T>C
  hgvsp: ENSP00000379579.1:p.Leu220Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.659T>C
  hgvsp: ENSP00000366310.1:p.Leu220Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.584T>C
  hgvsp: ENSP00000379581.1:p.Leu195Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.584T>C
  hgvsp: ENSP00000386127.2:p.Leu195Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1043T>C
  hgvsp: ENSP00000366314.2:p.Leu348Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.584T>C
  hgvsp: ENSP00000366309.1:p.Leu195Ser
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu348Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

9-73399134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399134
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399134
    reference: chr 9
allele count: 3
allele frequency: 2.479297862845242e-5
allele num: 121002
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.576G>A
  hgvsp: ENST00000396280.5:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.651G>A
  hgvsp: ENST00000396283.1:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.651G>A
  hgvsp: ENST00000377106.1:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.576G>A
  hgvsp: ENST00000361823.5:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.576G>A
  hgvsp: ENST00000408909.2:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1035G>A
  hgvsp: ENST00000377110.3:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.651G>A
  hgvsp: ENST00000396292.4:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.576G>A
  hgvsp: ENST00000377105.1:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.651G>A
  hgvsp: ENST00000360823.2:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1035G>A
  hgvsp: ENST00000377111.2:c.1035G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.651G>A
  hgvsp: ENST00000358082.3:c.651G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.576G>A
  hgvsp: ENST00000396285.1:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1116G>A
  hgvsp: ENST00000423814.3:c.1116G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1041G>A
  hgvsp: ENST00000357533.2:c.1041G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.576G>A
  hgvsp: ENST00000377101.1:c.576G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser345Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

9-73399163-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399163
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399163
    reference: chr 9
allele count: 2
allele frequency: 1.663284654535777e-5
allele num: 120244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.547A>G
  hgvsp: ENSP00000379581.1:p.Ile183Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1087A>G
  hgvsp: ENSP00000389542.3:p.Ile363Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1006A>G
  hgvsp: ENSP00000366314.2:p.Ile336Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.622A>G
  hgvsp: ENSP00000350791.3:p.Ile208Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.622A>G
  hgvsp: ENSP00000379587.4:p.Ile208Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.547A>G
  hgvsp: ENSP00000386127.2:p.Ile183Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.622A>G
  hgvsp: ENSP00000366310.1:p.Ile208Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.622A>G
  hgvsp: ENSP00000354066.2:p.Ile208Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.547A>G
  hgvsp: ENSP00000355395.4:p.Ile183Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1012A>G
  hgvsp: ENSP00000350140.2:p.Ile338Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1006A>G
  hgvsp: ENSP00000366315.2:p.Ile336Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.547A>G
  hgvsp: ENSP00000366305.1:p.Ile183Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.622A>G
  hgvsp: ENSP00000379579.1:p.Ile208Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.547A>G
  hgvsp: ENSP00000366309.1:p.Ile183Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.547A>G
  hgvsp: ENSP00000379576.5:p.Ile183Val
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27989
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile336Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

9-73399164-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399164
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399164
    reference: chr 9
allele count: 1
allele frequency: 8.320298199487469e-6
allele num: 120188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.546C>T
  hgvsp: ENST00000396280.5:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1086C>T
  hgvsp: ENST00000423814.3:c.1086C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.546C>T
  hgvsp: ENST00000408909.2:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.546C>T
  hgvsp: ENST00000377101.1:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.621C>T
  hgvsp: ENST00000396292.4:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.546C>T
  hgvsp: ENST00000396285.1:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1005C>T
  hgvsp: ENST00000377110.3:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.546C>T
  hgvsp: ENST00000377105.1:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.621C>T
  hgvsp: ENST00000358082.3:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.546C>T
  hgvsp: ENST00000361823.5:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.621C>T
  hgvsp: ENST00000377106.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1011C>T
  hgvsp: ENST00000357533.2:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.621C>T
  hgvsp: ENST00000396283.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.621C>T
  hgvsp: ENST00000360823.2:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1005C>T
  hgvsp: ENST00000377111.2:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu335Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

9-73399167-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399167
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399167
    reference: chr 9
allele count: 1
allele frequency: 8.336112037345782e-6
allele num: 119960
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.618A>G
  hgvsp: ENST00000358082.3:c.618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.618A>G
  hgvsp: ENST00000396292.4:c.618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.543A>G
  hgvsp: ENST00000396285.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.543A>G
  hgvsp: ENST00000408909.2:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1008A>G
  hgvsp: ENST00000357533.2:c.1008A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.618A>G
  hgvsp: ENST00000360823.2:c.618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.618A>G
  hgvsp: ENST00000377106.1:c.618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.543A>G
  hgvsp: ENST00000396280.5:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.543A>G
  hgvsp: ENST00000361823.5:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.618A>G
  hgvsp: ENST00000396283.1:c.618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.543A>G
  hgvsp: ENST00000377105.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.543A>G
  hgvsp: ENST00000377101.1:c.543A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1002A>G
  hgvsp: ENST00000377110.3:c.1002A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1083A>G
  hgvsp: ENST00000423814.3:c.1083A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1002A>G
  hgvsp: ENST00000377111.2:c.1002A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala334Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

9-73399168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399168
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399168
    reference: chr 9
allele count: 2
allele frequency: 1.669672076404194e-5
allele num: 119784
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.542C>T
  hgvsp: ENSP00000379576.5:p.Ala181Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.617C>T
  hgvsp: ENSP00000350791.3:p.Ala206Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.617C>T
  hgvsp: ENSP00000379587.4:p.Ala206Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.542C>T
  hgvsp: ENSP00000366305.1:p.Ala181Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.617C>T
  hgvsp: ENSP00000354066.2:p.Ala206Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.542C>T
  hgvsp: ENSP00000355395.4:p.Ala181Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.542C>T
  hgvsp: ENSP00000386127.2:p.Ala181Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1082C>T
  hgvsp: ENSP00000389542.3:p.Ala361Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.617C>T
  hgvsp: ENSP00000366310.1:p.Ala206Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.542C>T
  hgvsp: ENSP00000379581.1:p.Ala181Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.617C>T
  hgvsp: ENSP00000379579.1:p.Ala206Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.542C>T
  hgvsp: ENSP00000366309.1:p.Ala181Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.1001C>T
  hgvsp: ENSP00000366315.2:p.Ala334Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.1007C>T
  hgvsp: ENSP00000350140.2:p.Ala336Val
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.1001C>T
  hgvsp: ENSP00000366314.2:p.Ala334Val
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala334Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-73399190-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399190
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399190
    reference: chr 9
allele count: 1
allele frequency: 8.910591128615473e-6
allele num: 112226
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.595G>A
  hgvsp: ENSP00000354066.2:p.Gly199Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.520G>A
  hgvsp: ENSP00000355395.4:p.Gly174Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.979G>A
  hgvsp: ENSP00000366314.2:p.Gly327Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.595G>A
  hgvsp: ENSP00000379579.1:p.Gly199Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.595G>A
  hgvsp: ENSP00000379587.4:p.Gly199Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.595G>A
  hgvsp: ENSP00000350791.3:p.Gly199Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.520G>A
  hgvsp: ENSP00000366309.1:p.Gly174Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.520G>A
  hgvsp: ENSP00000366305.1:p.Gly174Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.520G>A
  hgvsp: ENSP00000379576.5:p.Gly174Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.595G>A
  hgvsp: ENSP00000366310.1:p.Gly199Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.985G>A
  hgvsp: ENSP00000350140.2:p.Gly329Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.520G>A
  hgvsp: ENSP00000379581.1:p.Gly174Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.979G>A
  hgvsp: ENSP00000366315.2:p.Gly327Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1060G>A
  hgvsp: ENSP00000389542.3:p.Gly354Ser
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.520G>A
  hgvsp: ENSP00000386127.2:p.Gly174Ser
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly327Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

9-73399200-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399200
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399200
    reference: chr 9
allele count: 1
allele frequency: 9.915519771546425e-6
allele num: 100852
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-5T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-5T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17407
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.974-5T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

9-73399208-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399208
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399208
    reference: chr 9
allele count: 1
allele frequency: 1.102244169128345e-5
allele num: 90724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-13T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-13T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

9-73399210-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399210
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399209
    reference: chr 9
allele count: 1
allele frequency: 1.134095445472691e-5
allele num: 88176
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-16delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-16delT
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25028
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: GA
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

9-73399216-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399216
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399216
    reference: chr 9
allele count: 2
allele frequency: 2.536912070627632e-5
allele num: 78836
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-21T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-21T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

9-73399219-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399219
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399219
    reference: chr 9
allele count: 1
allele frequency: 1.268552581504503e-5
allele num: 78830
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-24T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-24T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff

9-73399221-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399221
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399222
    reference: chr 9
allele count: 473
allele frequency: 6.736740158377485e-3
allele num: 70212
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-27dupT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-27dupT
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16783
  bin: 7.5e0
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 24757
  bin: 1.25e1
  variant carriers: 250
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 24
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/9-73399226-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399226
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399226
    reference: chr 9
allele count: 1
allele frequency: 1.449863712810996e-5
allele num: 68972
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-31T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-31T>G
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23818
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

9-73399227-AAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399227
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399225
    reference: chr 9
allele count: 1
allele frequency: 1.477672370482017e-5
allele num: 67674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-34_590-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-34_590-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-34_515-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-34_974-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-34_590-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-34_980-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-34_590-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-34_515-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-34_515-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-34_1055-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-34_515-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-34_590-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-34_515-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-34_974-33delCT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-34_515-33delCT
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4717
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: AAG
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

9-73399235-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73399235
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73399235
    reference: chr 9
allele count: 1
allele frequency: 1.710454296661193e-5
allele num: 58464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-40T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-40T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22054
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

9-73408451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408451
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408451
    reference: chr 9
allele count: 1
allele frequency: 6.941552131056504e-5
allele num: 14406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9256T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9256T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-73408467-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408467
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408467
    reference: chr 9
allele count: 11
allele frequency: 7.216900669203516e-4
allele num: 15242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9272T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9272T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/9-73408478-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408478
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408478
    reference: chr 9
allele count: 1
allele frequency: 6.289308176100629e-5
allele num: 15900
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9283G>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9283G>T
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

9-73408495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408495
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408495
    reference: chr 9
allele count: 3
allele frequency: 1.796837565884044e-4
allele num: 16696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9300G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9300G>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

9-73408496-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408496
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408496
    reference: chr 9
allele count: 3
allele frequency: 1.792114695340502e-4
allele num: 16740
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9301T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9301T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

9-73408518-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408518
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408518
    reference: chr 9
allele count: 13148
allele frequency: 7.567629791642685e-1
allele num: 17374
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9323A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9323A>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.25e1
  variant carriers: 603
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.75e1
  variant carriers: 575
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 6.25e1
  variant carriers: 574
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 412
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 2.5e0
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 2.25e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 5.75e1
  variant carriers: 609
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 345
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 8.75e1
  variant carriers: 383
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.25e1
  variant carriers: 526
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 101
genotype quality: GenotypeQuality
num of homozygotes: 5013
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

9-73408534-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408534
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408534
    reference: chr 9
allele count: 1
allele frequency: 5.770340450086555e-5
allele num: 17330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9339G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9339G>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

9-73408555-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408555
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408555
    reference: chr 9
allele count: 2
allele frequency: 1.15700566932778e-4
allele num: 17286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9360T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9360T>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

9-73408588-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408588
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408588
    reference: chr 9
allele count: 5
allele frequency: 2.917493289765433e-4
allele num: 17138
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9393T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9393T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

9-73408598-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408598
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408598
    reference: chr 9
allele count: 10
allele frequency: 5.881660981061052e-4
allele num: 17002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9403A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9403A>G
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

9-73408607-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408607
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408607
    reference: chr 9
allele count: 2
allele frequency: 1.1883541295306e-4
allele num: 16830
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9412A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9412A>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/9-73408609-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408609
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408609
    reference: chr 9
allele count: 2
allele frequency: 1.192890373374687e-4
allele num: 16766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9414T>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9414T>G
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

9-73408616-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408616
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408616
    reference: chr 9
allele count: 1
allele frequency: 6.007449237053947e-5
allele num: 16646
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9421C>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9421C>T
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD

9-73408650-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408650
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408650
    reference: chr 9
allele count: 3708
allele frequency: 2.347132548423851e-1
allele num: 15798
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9455T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9455T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 1.75e1
  variant carriers: 740
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 2.5e0
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 1.25e1
  variant carriers: 363
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 2.75e1
  variant carriers: 467
genotype quality: GenotypeQuality
num of homozygotes: 486
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

9-73408662-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73408662
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73408662
    reference: chr 9
allele count: 2
allele frequency: 1.313370107696349e-4
allele num: 15228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.515-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.974-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.515-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.590-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.590-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.974-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.515-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.515-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.590-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.590-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.515-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.590-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.980-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1055-9467A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.515-9467A>G
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

9-73424842-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424842
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424842
    reference: chr 9
allele count: 3
allele frequency: 2.489998506000897e-5
allele num: 120482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1244A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17921A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17921A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1244A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17921A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17921A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17921A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1244A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17921A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17921A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1244A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17921A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17921A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1244A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1244A>T
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

9-73424843-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424843
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424843
    reference: chr 9
allele count: 1
allele frequency: 8.307165761185599e-6
allele num: 120378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17920G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17920G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1243G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1243G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17920G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17920G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17920G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17920G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17920G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1243G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1243G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17920G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1243G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1243G>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17920G>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

9-73424844-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424844
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424844
    reference: chr 9
allele count: 1
allele frequency: 8.300270588821196e-6
allele num: 120478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17919T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17919T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17919T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1242T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17919T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1242T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17919T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17919T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17919T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17919T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1242T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1242T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1242T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17919T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1242T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

9-73424845-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424845
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424845
    reference: chr 9
allele count: 1
allele frequency: 8.301648707433296e-6
allele num: 120458
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1241A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1241A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17918A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17918A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1241A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1241A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17918A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17918A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17918A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17918A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17918A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17918A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1241A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1241A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17918A>G
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

9-73424851-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424851
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424851
    reference: chr 9
allele count: 1
allele frequency: 8.298617450332775e-6
allele num: 120502
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1235A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1235A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17912A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1235A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17912A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17912A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17912A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17912A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1235A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17912A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1235A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17912A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1235A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17912A>T
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17912A>T
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14649
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

9-73424854-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424854
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424854
    reference: chr 9
allele count: 1
allele frequency: 8.299168423323983e-6
allele num: 120494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17909G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1232G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17909G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17909G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17909G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1232G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1232G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17909G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17909G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1232G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17909G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1232G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17909G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17909G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1232G>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

9-73424855-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424855
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424855
    reference: chr 9
allele count: 17
allele frequency: 1.410343626076424e-4
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17908T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17908T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1231T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1231T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17908T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1231T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1231T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17908T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17908T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1231T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17908T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17908T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17908T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1231T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17908T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

9-73424856-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424856
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424856
    reference: chr 9
allele count: 1
allele frequency: 8.296001327360212e-6
allele num: 120540
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1230T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17907T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17907T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17907T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17907T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17907T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1230T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1230T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17907T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17907T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1230T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1230T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1230T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17907T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17907T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

9-73424856-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424856
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424856
    reference: chr 9
allele count: 1
allele frequency: 8.296001327360212e-6
allele num: 120540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1230T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1230T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1230T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17907T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17907T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1230T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17907T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17907T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17907T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1230T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17907T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17907T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1230T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17907T>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17907T>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

9-73424869-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424869
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424869
    reference: chr 9
allele count: 3
allele frequency: 2.487232207998939e-5
allele num: 120616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17894A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17894A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17894A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17894A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17894A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17894A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1217A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1217A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1217A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1217A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17894A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1217A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17894A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1217A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17894A>G
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

9-73424871-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424871
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424871
    reference: chr 9
allele count: 2
allele frequency: 1.657852417977751e-5
allele num: 120638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1215C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1215C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17892C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17892C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17892C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17892C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17892C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17892C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17892C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1215C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1215C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17892C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1215C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17892C>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1215C>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

9-73424881-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424881
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424881
    reference: chr 9
allele count: 2
allele frequency: 1.656643970644269e-5
allele num: 120726
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1205G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17882G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17882G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1205G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17882G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17882G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17882G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1205G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17882G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1205G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1205G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17882G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17882G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1205G>A
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17882G>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

9-73424883-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424883
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424883
    reference: chr 9
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17880T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17880T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17880T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17880T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1203T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17880T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17880T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1203T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1203T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1203T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17880T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17880T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1203T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17880T>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1203T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23706
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/9-73424893-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424893
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424892
    reference: chr 9
allele count: 3
allele frequency: 2.482703829984442e-5
allele num: 120836
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207935
  ensembl transcript: ENST00000385200
  gene symbol: MIR204
  hgvsc: ENST00000385200.1:n.107delT
  variant of: http://identifiers.org/hgnc/31582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17869delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17869delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17869delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17869delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1192delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17869delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17869delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1192delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1192delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17869delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1192delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1192delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17869delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1192delT
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17869delT
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: CA
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

9-73424905-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424905
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424905
    reference: chr 9
allele count: 17
allele frequency: 1.406399947053178e-4
allele num: 120876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17858A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1181A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1181A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1181A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17858A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17858A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17858A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207935
  ensembl transcript: ENST00000385200
  gene symbol: MIR204
  hgvsc: ENST00000385200.1:n.96A>G
  variant of: http://identifiers.org/hgnc/31582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17858A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1181A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17858A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17858A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1181A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1181A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17858A>G
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17858A>G
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

9-73424905-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424905
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424905
    reference: chr 9
allele count: 2
allele frequency: 1.654588173003739e-5
allele num: 120876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.589+1181A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.514+17858A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.589+1181A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.514+17858A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379579
  ensembl transcript: ENST00000396283
  gene symbol: TRPM3
  hgvsc: ENST00000396283.1:c.589+1181A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207935
  ensembl transcript: ENST00000385200
  gene symbol: MIR204
  hgvsc: ENST00000385200.1:n.96A>C
  variant of: http://identifiers.org/hgnc/31582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.979+17858A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.973+17858A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.514+17858A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.1054+1181A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.514+17858A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.589+1181A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.973+17858A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.589+1181A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366305
  ensembl transcript: ENST00000377101
  gene symbol: TRPM3
  hgvsc: ENST00000377101.1:c.514+17858A>C
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000355395
  ensembl transcript: ENST00000361823
  gene symbol: TRPM3
  hgvsc: ENST00000361823.5:c.514+17858A>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

9-73424910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73424910
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73424910
allele count: 125
allele frequency: 1.034066279512252e-3
allele num: 120882
alternate allele: T
canonical: true
consequence: non coding transcript exon
filter: PASS
num of homozygotes: 3
reference allele: C

GenotypeDepth
all individuals: 197
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 768
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 299
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 57
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 137
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1474
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43359
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8234
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.060798933139359e-4
allele num: 65988
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: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14610
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.374e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 1.721883e6

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

GenotypeDepth
all individuals: 219
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2785
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 90
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44301
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8304
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1764
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1464
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66304
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15280
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e0

DP
type: SiteQuality
SIO_000300: 1.735647e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 1.202e1

GenotypeDepth
all individuals: 2786
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 109
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 769
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 28031
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15345
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 196
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

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

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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50665943470138e-5
allele num: 66372
num of homozygotes: 0

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

African
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allele 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

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

MQRankSum
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SIO_000300: -1.0e-2

BaseQRankSum
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SIO_000300: 3.71e0

DP
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SIO_000300: 1.740363e6

VQSLOD
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SIO_000300: 8.0e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

FS
type: SiteQuality
SIO_000300: 3.67e-1

ReadPosRankSum
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SIO_000300: 1.57e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-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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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
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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

African
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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: 2
allele frequency: 3.01050666827227e-5
allele num: 66434
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

Other
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num of homozygotes: 0

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -1.39e-1

BaseQRankSum
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SIO_000300: 1.82e0

DP
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SIO_000300: 1.744618e6

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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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: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.318034306907742e-4
allele num: 8628
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15948
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

QD
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SIO_000300: 6.77e0

ReadPosRankSum
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SIO_000300: 1.57e0

BaseQRankSum
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SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.48e-1

FS
type: SiteQuality
SIO_000300: 2.933e0

VQSLOD
type: SiteQuality
SIO_000300: -7.055e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 1.748968e6

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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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 (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503533303262667e-5
allele num: 66510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: -4.04e-1

InbreedingCoeff
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VQSLOD
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FS
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DP
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 4.04e-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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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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allele count: 9
allele frequency: 8.648856428983279e-4
allele num: 10406
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
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Other
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European (Non-Finnish)
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allele num: 66686
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East Asian
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South Asian
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
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DP
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
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South Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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FS
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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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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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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South Asian
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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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European (Non-Finnish)
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allele num: 66696
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African
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Other
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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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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Latino
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allele frequency: 8.677542519958348e-5
allele num: 11524
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele count: 0
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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Other
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
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SIO_000300: 5.669999999999999e-1

FS
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SIO_000300: 8.74e-1

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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European (Non-Finnish)
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allele num: 66700
num of homozygotes: 0

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

Latino
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African
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South Asian
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ClippingRankSum
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SIO_000300: -5.23e-1

VQSLOD
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FS
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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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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African
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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allele count: 1
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allele num: 66696
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East Asian
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Latino
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South Asian
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Other
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ClippingRankSum
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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African
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South Asian
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Latino
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Other
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European (Finnish)
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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FS
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QD
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MQ
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ClippingRankSum
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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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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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South Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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Latino
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East Asian
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African
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QD
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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DP
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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African
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Other
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European (Finnish)
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East Asian
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InbreedingCoeff
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VQSLOD
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DP
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FS
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QD
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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South Asian
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Latino
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Other
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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FS
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QD
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

Latino
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Other
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East Asian
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African
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Latino
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Other
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BaseQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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South Asian
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European (Finnish)
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Other
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FS
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DP
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MQRankSum
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SIO_000300: 5.04e-1

ReadPosRankSum
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MQ
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BaseQRankSum
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SIO_000300: -2.204e0

VQSLOD
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InbreedingCoeff
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SIO_000300: -4.0e-4

ClippingRankSum
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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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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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66186
num of homozygotes: 0

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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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 9.665571235260003e-5
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South Asian
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Other
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allele frequency: 0.0e0
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MQRankSum
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DP
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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QD
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GenotypeDepth
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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 (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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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.513546238837597e-5
allele num: 66070
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 frequency: 0.0e0
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South Asian
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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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FS
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SIO_000300: 0.0e0

VQSLOD
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ReadPosRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
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SIO_000300: -4.0e-4

MQRankSum
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SIO_000300: -2.02e-1

BaseQRankSum
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SIO_000300: 2.44e0

DP
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SIO_000300: 1.721724e6

ClippingRankSum
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SIO_000300: -5.11e-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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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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African
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South Asian
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Latino
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European (Finnish)
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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FS
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InbreedingCoeff
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VQSLOD
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DP
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QD
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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African
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South Asian
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Other
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European (Non-Finnish)
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Latino
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FS
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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BaseQRankSum
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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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GenotypeQuality
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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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African
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European (Non-Finnish)
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Other
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European (Finnish)
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East Asian
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ClippingRankSum
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DP
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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Latino
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South Asian
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.27e-1

FS
type: SiteQuality
SIO_000300: 7.014e0

VQSLOD
type: SiteQuality
SIO_000300: 3.19e-1

DP
type: SiteQuality
SIO_000300: 9.97498e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

QD
type: SiteQuality
SIO_000300: 1.532e1

MQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 12224
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.766160367361356e-4
allele num: 5662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 3.163e0

ClippingRankSum
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SIO_000300: -2.67e-1

ReadPosRankSum
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SIO_000300: -5.4e-1

MQ
type: SiteQuality
SIO_000300: 6.113e1

MQRankSum
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SIO_000300: -1.5e-2

BaseQRankSum
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SIO_000300: 4.75e-1

DP
type: SiteQuality
SIO_000300: 9.61572e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.3e-3

QD
type: SiteQuality
SIO_000300: 1.173e1

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.556016219417741e-5
allele num: 43898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.44e0

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

DP
type: SiteQuality
SIO_000300: 8.4407e5

VQSLOD
type: SiteQuality
SIO_000300: -1.031e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

MQ
type: SiteQuality
SIO_000300: 5.878e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.95e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 287
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.946144211844694e-5
allele num: 11178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43812
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.271e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

VQSLOD
type: SiteQuality
SIO_000300: -1.291e0

QD
type: SiteQuality
SIO_000300: 1.478e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.032e0

MQRankSum
type: SiteQuality
SIO_000300: -1.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.40768e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-2

GenotypeDepth
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variant carriers: 37

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 112

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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variant carriers: 343

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 17

GenotypeQuality
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GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 28

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5214
num of homozygotes: 0

East Asian
type: Population
allele count: 461
allele frequency: 1.089319470699433e-1
allele num: 4232
num of homozygotes: 24

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.01295570955107e-4
allele num: 6638
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 9.966115208291809e-4
allele num: 10034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.192e1

BaseQRankSum
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ClippingRankSum
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SIO_000300: 3.9e-2

ReadPosRankSum
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MQRankSum
type: SiteQuality
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FS
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DP
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.067e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5038
num of homozygotes: 0

European (Finnish)
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: 38454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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East Asian
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allele count: 1
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allele num: 3980
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QD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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MQ
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 189
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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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

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: 1
allele frequency: 2.646342754313539e-5
allele num: 37788
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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QD
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MQ
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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FS
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BaseQRankSum
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SIO_000300: 9.26e-1

ClippingRankSum
type: SiteQuality
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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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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Other
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South Asian
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Latino
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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South Asian
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African
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Other
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QD
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FS
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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South Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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FS
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Latino
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East Asian
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African
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Other
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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MQ
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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South Asian
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Other
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MQRankSum
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VQSLOD
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ClippingRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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FS
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DP
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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Latino
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South Asian
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European (Finnish)
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East Asian
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African
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 84
bin: 9.25e1
variant carriers: 77

GenotypeQuality
all individuals: 81
bin: 7.75e1
variant carriers: 68

GenotypeQuality
all individuals: 80
bin: 8.25e1
variant carriers: 73

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 15

GenotypeQuality
all individuals: 156
bin: 1.75e1
variant carriers: 151

GenotypeQuality
all individuals: 140
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 44

GenotypeQuality
all individuals: 307
bin: 7.5e0
variant carriers: 158

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 33

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 18

GenotypeQuality
all individuals: 7727
bin: 9.75e1
variant carriers: 7689

GenotypeQuality
all individuals: 456
bin: 6.25e1
variant carriers: 42

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 77

GenotypeQuality
all individuals: 54
bin: 8.75e1
variant carriers: 48

Latino
type: Population
allele count: 218
allele frequency: 7.364864864864865e-1
allele num: 296
num of homozygotes: 80

East Asian
type: Population
allele count: 344
allele frequency: 7.107438016528925e-1
allele num: 484
num of homozygotes: 122

European (Non-Finnish)
type: Population
allele count: 4705
allele frequency: 7.836442371752165e-1
allele num: 6004
num of homozygotes: 1831

African
type: Population
allele count: 616
allele frequency: 5.724907063197026e-1
allele num: 1076
num of homozygotes: 171

Other
type: Population
allele count: 170
allele frequency: 8.018867924528302e-1
allele num: 212
num of homozygotes: 67

South Asian
type: Population
allele count: 5834
allele frequency: 7.610226976258805e-1
allele num: 7666
num of homozygotes: 2255

European (Finnish)
type: Population
allele count: 1261
allele frequency: 7.707823960880196e-1
allele num: 1636
num of homozygotes: 487

FS
type: SiteQuality
SIO_000300: 6.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

DP
type: SiteQuality
SIO_000300: 5.99847e5

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.54e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

QD
type: SiteQuality
SIO_000300: 2.714e1

GenotypeDepth
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1302
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1605
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variant carriers: 0

GenotypeDepth
all individuals: 84
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variant carriers: 0

GenotypeDepth
all individuals: 76
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variant carriers: 0

GenotypeDepth
all individuals: 53
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variant carriers: 0

GenotypeDepth
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 1154
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 4915
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
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GenotypeQuality
all individuals: 345
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 4.807692307692308e-3
allele num: 208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.31e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.336e-1

DP
type: SiteQuality
SIO_000300: 2.98223e5

MQ
type: SiteQuality
SIO_000300: 5.871e1

GenotypeDepth
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
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variant carriers: 0

GenotypeDepth
all individuals: 158
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variant carriers: 0

GenotypeDepth
all individuals: 556
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variant carriers: 0

GenotypeDepth
all individuals: 112
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variant carriers: 0

GenotypeDepth
all individuals: 120
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variant carriers: 0

GenotypeDepth
all individuals: 76
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variant carriers: 0

GenotypeDepth
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
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variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4931
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1358
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 178
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.86219739292365e-3
allele num: 1074
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.71e-1

FS
type: SiteQuality
SIO_000300: 7.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.35e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 2.97713e5

VQSLOD
type: SiteQuality
SIO_000300: 5.620000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.56e-2

QD
type: SiteQuality
SIO_000300: 1.056e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.05e-1

GenotypeDepth
all individuals: 178
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 53
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
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variant carriers: 0

GenotypeDepth
all individuals: 146
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variant carriers: 0

GenotypeDepth
all individuals: 1525
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variant carriers: 2

GenotypeDepth
all individuals: 84
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variant carriers: 1

GenotypeDepth
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 328
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GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1205
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GenotypeQuality
all individuals: 1356
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1139
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 548
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
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variant carriers: 0

GenotypeQuality
all individuals: 113
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 4817
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variant carriers: 0

GenotypeQuality
all individuals: 172
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variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1626
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5830
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.854368932038835e-3
allele num: 1030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.826e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 5.05e-1

QD
type: SiteQuality
SIO_000300: 1.199e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

DP
type: SiteQuality
SIO_000300: 2.9429e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

GenotypeDepth
all individuals: 94
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 495
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3473
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1505
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 84
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variant carriers: 1

GenotypeDepth
all individuals: 113
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.5e0
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GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 7.5e0
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GenotypeQuality
all individuals: 579
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variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 1357
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variant carriers: 10

GenotypeQuality
all individuals: 1102
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 325
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GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 4681
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GenotypeQuality
all individuals: 111
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 327
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1624
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.881422924901186e-3
allele num: 1012
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5742
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

FS
type: SiteQuality
SIO_000300: 5.232e0

QD
type: SiteQuality
SIO_000300: 1.274e1

DP
type: SiteQuality
SIO_000300: 2.90871e5

GenotypeDepth
all individuals: 161
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 120
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 119
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variant carriers: 0

GenotypeDepth
all individuals: 53
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variant carriers: 0

GenotypeDepth
all individuals: 314
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GenotypeDepth
all individuals: 94
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GenotypeDepth
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 116
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GenotypeQuality
all individuals: 159
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
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GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.75e1
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GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 1246
bin: 7.5e0
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GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 4479
bin: 6.25e1
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GenotypeQuality
all individuals: 314
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GenotypeQuality
all individuals: 50
bin: 1.25e1
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GenotypeQuality
all individuals: 626
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
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GenotypeQuality
all individuals: 1345
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 109
bin: 9.25e1
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GenotypeQuality
all individuals: 1056
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.631578947368421e-4
allele num: 7600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.601e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.65e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.861e1

MQRankSum
type: SiteQuality
SIO_000300: 2.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
type: SiteQuality
SIO_000300: -2.195e0

DP
type: SiteQuality
SIO_000300: 2.85589e5

GenotypeDepth
all individuals: 111
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3300
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variant carriers: 0

GenotypeDepth
all individuals: 504
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GenotypeDepth
all individuals: 160
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GenotypeDepth
all individuals: 53
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GenotypeDepth
all individuals: 83
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GenotypeDepth
all individuals: 120
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GenotypeDepth
all individuals: 44
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GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 52
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GenotypeQuality
all individuals: 661
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GenotypeQuality
all individuals: 156
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GenotypeQuality
all individuals: 129
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GenotypeQuality
all individuals: 1021
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GenotypeQuality
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GenotypeQuality
all individuals: 4359
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GenotypeQuality
all individuals: 53
bin: 1.75e1
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GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 7.5e0
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GenotypeQuality
all individuals: 48
bin: 5.25e1
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GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 103
bin: 2.75e1
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GenotypeQuality
all individuals: 312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 974
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.642007926023778e-4
allele num: 7570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 486
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.63e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 1.248e1

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

DP
type: SiteQuality
SIO_000300: 2.83286e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

FS
type: SiteQuality
SIO_000300: 9.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.282e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

GenotypeDepth
all individuals: 577
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 111
bin: 6.75e1
variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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bin: 6.25e1
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GenotypeDepth
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5550
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.0351966873706e-3
allele num: 966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.77778e5

MQRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.278e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.062e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.63e-1

MQ
type: SiteQuality
SIO_000300: 5.884e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-2

FS
type: SiteQuality
SIO_000300: 3.646e0

QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeDepth
all individuals: 92
bin: 7.25e1
variant carriers: 36

GenotypeDepth
all individuals: 1450
bin: 2.25e1
variant carriers: 787

GenotypeDepth
all individuals: 150
bin: 4.25e1
variant carriers: 73

GenotypeDepth
all individuals: 467
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variant carriers: 230

GenotypeDepth
all individuals: 50
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variant carriers: 23

GenotypeDepth
all individuals: 83
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variant carriers: 36

GenotypeDepth
all individuals: 147
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variant carriers: 52

GenotypeDepth
all individuals: 117
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variant carriers: 48

GenotypeQuality
all individuals: 416
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variant carriers: 1

GenotypeQuality
all individuals: 352
bin: 2.75e1
variant carriers: 19

GenotypeQuality
all individuals: 1065
bin: 7.5e0
variant carriers: 38

GenotypeQuality
all individuals: 111
bin: 7.25e1
variant carriers: 37

GenotypeQuality
all individuals: 238
bin: 4.25e1
variant carriers: 18

GenotypeQuality
all individuals: 519
bin: 3.75e1
variant carriers: 30

GenotypeQuality
all individuals: 769
bin: 2.25e1
variant carriers: 20

GenotypeQuality
all individuals: 3604
bin: 9.75e1
variant carriers: 2802

GenotypeQuality
all individuals: 80
bin: 8.75e1
variant carriers: 45

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 55

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 32

GenotypeQuality
all individuals: 585
bin: 3.25e1
variant carriers: 20

GenotypeQuality
all individuals: 145
bin: 7.75e1
variant carriers: 58

GenotypeQuality
all individuals: 127
bin: 1.25e1
variant carriers: 24

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 33

GenotypeQuality
all individuals: 269
bin: 6.75e1
variant carriers: 50

GenotypeQuality
all individuals: 74
bin: 9.25e1
variant carriers: 34

GenotypeQuality
all individuals: 283
bin: 4.75e1
variant carriers: 52

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 23

GenotypeQuality
all individuals: 1033
bin: 6.25e1
variant carriers: 71

East Asian
type: Population
allele count: 229
allele frequency: 4.790794979079498e-1
allele num: 478
num of homozygotes: 53

Latino
type: Population
allele count: 93
allele frequency: 3.229166666666667e-1
allele num: 288
num of homozygotes: 15

South Asian
type: Population
allele count: 1939
allele frequency: 2.699805068226121e-1
allele num: 7182
num of homozygotes: 267

European (Finnish)
type: Population
allele count: 319
allele frequency: 1.971569839307787e-1
allele num: 1618
num of homozygotes: 33

Other
type: Population
allele count: 50
allele frequency: 2.577319587628866e-1
allele num: 194
num of homozygotes: 9

African
type: Population
allele count: 72
allele frequency: 8.01781737193764e-2
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1006
allele frequency: 1.957198443579767e-1
allele num: 5140
num of homozygotes: 109

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e-1

QD
type: SiteQuality
SIO_000300: 1.891e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.34e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

DP
type: SiteQuality
SIO_000300: 2.33398e5

GenotypeDepth
all individuals: 91
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 608
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
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variant carriers: 0

GenotypeDepth
all individuals: 159
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variant carriers: 0

GenotypeDepth
all individuals: 900
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variant carriers: 0

GenotypeDepth
all individuals: 147
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variant carriers: 0

GenotypeDepth
all individuals: 150
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variant carriers: 0

GenotypeQuality
all individuals: 960
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variant carriers: 0

GenotypeQuality
all individuals: 730
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variant carriers: 0

GenotypeQuality
all individuals: 352
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variant carriers: 0

GenotypeQuality
all individuals: 960
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variant carriers: 0

GenotypeQuality
all individuals: 579
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variant carriers: 0

GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
all individuals: 429
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variant carriers: 0

GenotypeQuality
all individuals: 505
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GenotypeQuality
all individuals: 205
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variant carriers: 0

GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
all individuals: 265
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GenotypeQuality
all individuals: 146
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GenotypeQuality
all individuals: 1023
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variant carriers: 0

GenotypeQuality
all individuals: 1320
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GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 493
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GenotypeQuality
all individuals: 71
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GenotypeQuality
all individuals: 1253
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 56
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1618
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.94811320754717e-4
allele num: 6784
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.27e1

VQSLOD
type: SiteQuality
SIO_000300: -3.48e-1

DP
type: SiteQuality
SIO_000300: 2.11957e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.15e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.188e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e0

GenotypeDepth
all individuals: 334
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 22996
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variant carriers: 0

GenotypeDepth
all individuals: 403
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variant carriers: 1

GenotypeDepth
all individuals: 1450
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variant carriers: 0

GenotypeDepth
all individuals: 503
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variant carriers: 0

GenotypeDepth
all individuals: 224
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GenotypeDepth
all individuals: 1367
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variant carriers: 1

GenotypeDepth
all individuals: 2339
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variant carriers: 0

GenotypeQuality
all individuals: 343
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variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 9751
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 28537
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GenotypeQuality
all individuals: 3515
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GenotypeQuality
all individuals: 42
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GenotypeQuality
all individuals: 2325
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 399
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GenotypeQuality
all individuals: 1282
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1001
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GenotypeQuality
all individuals: 261
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.536930615207792e-5
allele num: 66124
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.991e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

QD
type: SiteQuality
SIO_000300: 1.528e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

DP
type: SiteQuality
SIO_000300: 2.045514e6

FS
type: SiteQuality
SIO_000300: 9.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1366
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 289
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variant carriers: 0

GenotypeDepth
all individuals: 14634
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GenotypeDepth
all individuals: 925
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GenotypeDepth
all individuals: 402
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GenotypeDepth
all individuals: 285
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GenotypeDepth
all individuals: 685
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GenotypeQuality
all individuals: 207
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1280
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GenotypeQuality
all individuals: 998
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66104
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.045593e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.268e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

FS
type: SiteQuality
SIO_000300: 4.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

GenotypeDepth
all individuals: 925
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1450
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variant carriers: 0

GenotypeDepth
all individuals: 214
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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
all individuals: 305
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GenotypeQuality
all individuals: 2320
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8028
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
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: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512172992590352e-5
allele num: 66130
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

Other
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allele count: 0
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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Latino
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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South Asian
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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African
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East Asian
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InbreedingCoeff
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DP
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MQ
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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African
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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African
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Latino
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East Asian
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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QD
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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SIO_000300: 1.5e-1

DP
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SIO_000300: 2.051586e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.022700480609376e-5
allele num: 66166
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.014e0

MQ
type: SiteQuality
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ClippingRankSum
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SIO_000300: -2.39e-1

InbreedingCoeff
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SIO_000300: 2.6e-3

VQSLOD
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ReadPosRankSum
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SIO_000300: 6.62e-1

DP
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SIO_000300: 2.058454e6

BaseQRankSum
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MQRankSum
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SIO_000300: 2.83e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.022517757291824e-5
allele num: 66170
num of homozygotes: 0

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

South Asian
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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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

MQRankSum
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ReadPosRankSum
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SIO_000300: 1.1e0

BaseQRankSum
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SIO_000300: -2.011e0

MQ
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SIO_000300: 5.96e1

QD
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SIO_000300: 9.1e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 4.18e-1

DP
type: SiteQuality
SIO_000300: 2.05917e6

VQSLOD
type: SiteQuality
SIO_000300: 1.1e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6614
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66202
num of homozygotes: 0

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

African
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allele count: 2
allele frequency: 1.933114247052001e-4
allele num: 10346
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: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.684e0

QD
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 7.58e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.064274e6

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510300247689241e-5
allele num: 66212
num of homozygotes: 0

Latino
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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

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

Other
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FS
type: SiteQuality
SIO_000300: 8.686999999999999e0

InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQ
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MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

DP
type: SiteQuality
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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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GenotypeDepth
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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: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 4.528575310207409e-5
allele num: 66246
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Latino
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num of homozygotes: 0

Other
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FS
type: SiteQuality
SIO_000300: 5.22e-1

BaseQRankSum
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MQ
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ClippingRankSum
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QD
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MQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10
allele frequency: 1.509023963300537e-4
allele num: 66268
num of homozygotes: 0

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

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

South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 6.046993780234969e-4
allele num: 11576
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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MQ
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ClippingRankSum
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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
all individuals: 284
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 329
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7682
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 23808
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3529
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2323
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9930
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8001
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1281
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1005
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31130
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66268
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.933114247052001e-4
allele num: 10346
num of homozygotes: 0

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

Other
type: Population
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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.37e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

DP
type: SiteQuality
SIO_000300: 2.067646e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1