9-73151381-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151381
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151381
    reference: chr 9
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
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.4159C>T
  hgvsp: ENSP00000379576.5:p.Pro1387Ser
  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.4228C>T
  hgvsp: ENSP00000379587.4:p.Pro1410Ser
  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.4624C>T
  hgvsp: ENSP00000350140.2:p.Pro1542Ser
  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.4198C>T
  hgvsp: ENSP00000350791.3:p.Pro1400Ser
  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.3955+657C>T
  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.4693C>T
  hgvsp: ENSP00000389542.3:p.Pro1565Ser
  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.4198C>T
  hgvsp: ENSP00000354066.2:p.Pro1400Ser
  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.4228C>T
  hgvsp: ENSP00000366310.1:p.Pro1410Ser
  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.4189C>T
  hgvsp: ENSP00000366309.1:p.Pro1397Ser
  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.4189C>T
  hgvsp: ENSP00000379581.1:p.Pro1397Ser
  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.4189C>T
  hgvsp: ENSP00000386127.2:p.Pro1397Ser
  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.4612C>T
  hgvsp: ENSP00000366314.2:p.Pro1538Ser
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1538Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/9-73151383-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151383
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151382
    reference: chr 9
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.4186delG
  hgvsp: ENSP00000379581.1:p.Val1396CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.4609delG
  hgvsp: ENSP00000366314.2:p.Val1537CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.4690delG
  hgvsp: ENSP00000389542.3:p.Val1564CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.4225delG
  hgvsp: ENSP00000379587.4:p.Val1409CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.4186delG
  hgvsp: ENSP00000366309.1:p.Val1396CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.4621delG
  hgvsp: ENSP00000350140.2:p.Val1541CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.4195delG
  hgvsp: ENSP00000350791.3:p.Val1399CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.4225delG
  hgvsp: ENSP00000366310.1:p.Val1409CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.4156delG
  hgvsp: ENSP00000379576.5:p.Val1386CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.4195delG
  hgvsp: ENSP00000354066.2:p.Val1399CysfsTer3
  variant of: http://identifiers.org/hgnc/17992
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.4186delG
  hgvsp: ENSP00000386127.2:p.Val1396CysfsTer3
  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.3955+654delG
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val1537CysfsTer3
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: AC
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-73151386-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151386
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151386
    reference: chr 9
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.4184G>T
  hgvsp: ENSP00000386127.2:p.Gly1395Val
  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.4154G>T
  hgvsp: ENSP00000379576.5:p.Gly1385Val
  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.4184G>T
  hgvsp: ENSP00000379581.1:p.Gly1395Val
  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.4193G>T
  hgvsp: ENSP00000354066.2:p.Gly1398Val
  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.4193G>T
  hgvsp: ENSP00000350791.3:p.Gly1398Val
  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.3955+652G>T
  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.4619G>T
  hgvsp: ENSP00000350140.2:p.Gly1540Val
  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.4223G>T
  hgvsp: ENSP00000366310.1:p.Gly1408Val
  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.4688G>T
  hgvsp: ENSP00000389542.3:p.Gly1563Val
  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.4223G>T
  hgvsp: ENSP00000379587.4:p.Gly1408Val
  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.4607G>T
  hgvsp: ENSP00000366314.2:p.Gly1536Val
  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.4184G>T
  hgvsp: ENSP00000366309.1:p.Gly1395Val
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2746
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1536Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

9-73151387-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151387
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151387
    reference: chr 9
allele count: 423
allele frequency: 3.485153083083413e-3
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.4192G>A
  hgvsp: ENSP00000350791.3:p.Gly1398Arg
  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.4606G>A
  hgvsp: ENSP00000366314.2:p.Gly1536Arg
  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.3955+651G>A
  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.4222G>A
  hgvsp: ENSP00000366310.1:p.Gly1408Arg
  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.4687G>A
  hgvsp: ENSP00000389542.3:p.Gly1563Arg
  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.4183G>A
  hgvsp: ENSP00000366309.1:p.Gly1395Arg
  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.4618G>A
  hgvsp: ENSP00000350140.2:p.Gly1540Arg
  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.4183G>A
  hgvsp: ENSP00000386127.2:p.Gly1395Arg
  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.4192G>A
  hgvsp: ENSP00000354066.2:p.Gly1398Arg
  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.4153G>A
  hgvsp: ENSP00000379576.5:p.Gly1385Arg
  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.4183G>A
  hgvsp: ENSP00000379581.1:p.Gly1395Arg
  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.4222G>A
  hgvsp: ENSP00000379587.4:p.Gly1408Arg
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 6.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 9.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 4554
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 6869
  bin: 9.75e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1536Arg
num of homozygotes: 7
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

9-73151398-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151398
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151398
    reference: chr 9
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
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.4181A>T
  hgvsp: ENSP00000350791.3:p.Tyr1394Phe
  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.4676A>T
  hgvsp: ENSP00000389542.3:p.Tyr1559Phe
  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.4172A>T
  hgvsp: ENSP00000379581.1:p.Tyr1391Phe
  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.4211A>T
  hgvsp: ENSP00000366310.1:p.Tyr1404Phe
  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.4142A>T
  hgvsp: ENSP00000379576.5:p.Tyr1381Phe
  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.3955+640A>T
  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.4181A>T
  hgvsp: ENSP00000354066.2:p.Tyr1394Phe
  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.4172A>T
  hgvsp: ENSP00000386127.2:p.Tyr1391Phe
  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.4607A>T
  hgvsp: ENSP00000350140.2:p.Tyr1536Phe
  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.4595A>T
  hgvsp: ENSP00000366314.2:p.Tyr1532Phe
  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.4211A>T
  hgvsp: ENSP00000379587.4:p.Tyr1404Phe
  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.4172A>T
  hgvsp: ENSP00000366309.1:p.Tyr1391Phe
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr1532Phe
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: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

9-73151404-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151404
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151404
    reference: chr 9
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.4670G>A
  hgvsp: ENSP00000389542.3:p.Ser1557Asn
  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.4175G>A
  hgvsp: ENSP00000350791.3:p.Ser1392Asn
  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.4205G>A
  hgvsp: ENSP00000379587.4:p.Ser1402Asn
  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.3955+634G>A
  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.4601G>A
  hgvsp: ENSP00000350140.2:p.Ser1534Asn
  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.4166G>A
  hgvsp: ENSP00000366309.1:p.Ser1389Asn
  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.4589G>A
  hgvsp: ENSP00000366314.2:p.Ser1530Asn
  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.4166G>A
  hgvsp: ENSP00000386127.2:p.Ser1389Asn
  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.4166G>A
  hgvsp: ENSP00000379581.1:p.Ser1389Asn
  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.4136G>A
  hgvsp: ENSP00000379576.5:p.Ser1379Asn
  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.4175G>A
  hgvsp: ENSP00000354066.2:p.Ser1392Asn
  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.4205G>A
  hgvsp: ENSP00000366310.1:p.Ser1402Asn
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4446
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1530Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/9-73151419-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151419
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151419
    reference: chr 9
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.4151T>G
  hgvsp: ENSP00000386127.2:p.Phe1384Cys
  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.4160T>G
  hgvsp: ENSP00000350791.3:p.Phe1387Cys
  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.4160T>G
  hgvsp: ENSP00000354066.2:p.Phe1387Cys
  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.4586T>G
  hgvsp: ENSP00000350140.2:p.Phe1529Cys
  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.4121T>G
  hgvsp: ENSP00000379576.5:p.Phe1374Cys
  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.4151T>G
  hgvsp: ENSP00000379581.1:p.Phe1384Cys
  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.4190T>G
  hgvsp: ENSP00000379587.4:p.Phe1397Cys
  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.3955+619T>G
  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.4190T>G
  hgvsp: ENSP00000366310.1:p.Phe1397Cys
  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.4574T>G
  hgvsp: ENSP00000366314.2:p.Phe1525Cys
  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.4151T>G
  hgvsp: ENSP00000366309.1:p.Phe1384Cys
  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.4655T>G
  hgvsp: ENSP00000389542.3:p.Phe1552Cys
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe1525Cys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

9-73151421-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151421
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151421
    reference: chr 9
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.4653G>A
  hgvsp: ENSP00000389542.3:p.Met1551Ile
  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.4188G>A
  hgvsp: ENSP00000379587.4:p.Met1396Ile
  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.4188G>A
  hgvsp: ENSP00000366310.1:p.Met1396Ile
  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.4119G>A
  hgvsp: ENSP00000379576.5:p.Met1373Ile
  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.4158G>A
  hgvsp: ENSP00000350791.3:p.Met1386Ile
  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.4584G>A
  hgvsp: ENSP00000350140.2:p.Met1528Ile
  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.4149G>A
  hgvsp: ENSP00000379581.1:p.Met1383Ile
  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.4149G>A
  hgvsp: ENSP00000366309.1:p.Met1383Ile
  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.4572G>A
  hgvsp: ENSP00000366314.2:p.Met1524Ile
  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.3955+617G>A
  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.4158G>A
  hgvsp: ENSP00000354066.2:p.Met1386Ile
  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.4149G>A
  hgvsp: ENSP00000386127.2:p.Met1383Ile
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1524Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

9-73151430-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151430
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151430
    reference: chr 9
allele count: 8
allele frequency: 6.595000989250148e-5
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.4149T>C
  hgvsp: ENST00000360823.2:c.4149T>C(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.4140T>C
  hgvsp: ENST00000408909.2:c.4140T>C(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.4140T>C
  hgvsp: ENST00000396285.1:c.4140T>C(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.4644T>C
  hgvsp: ENST00000423814.3:c.4644T>C(p.%3D)
  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.3955+608T>C
  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.4179T>C
  hgvsp: ENST00000396292.4:c.4179T>C(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.4110T>C
  hgvsp: ENST00000396280.5:c.4110T>C(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.4563T>C
  hgvsp: ENST00000377110.3:c.4563T>C(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.4575T>C
  hgvsp: ENST00000357533.2:c.4575T>C(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.4179T>C
  hgvsp: ENST00000377106.1:c.4179T>C(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.4149T>C
  hgvsp: ENST00000358082.3:c.4149T>C(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.4140T>C
  hgvsp: ENST00000377105.1:c.4140T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His1521His
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

9-73151446-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151446
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151446
    reference: chr 9
allele count: 2
allele frequency: 1.648994937585542e-5
allele num: 121286
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.4163C>T
  hgvsp: ENSP00000366310.1:p.Pro1388Leu
  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.3955+592C>T
  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.4133C>T
  hgvsp: ENSP00000354066.2:p.Pro1378Leu
  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.4124C>T
  hgvsp: ENSP00000366309.1:p.Pro1375Leu
  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.4124C>T
  hgvsp: ENSP00000379581.1:p.Pro1375Leu
  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.4094C>T
  hgvsp: ENSP00000379576.5:p.Pro1365Leu
  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.4559C>T
  hgvsp: ENSP00000350140.2:p.Pro1520Leu
  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.4133C>T
  hgvsp: ENSP00000350791.3:p.Pro1378Leu
  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.4163C>T
  hgvsp: ENSP00000379587.4:p.Pro1388Leu
  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.4547C>T
  hgvsp: ENSP00000366314.2:p.Pro1516Leu
  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.4628C>T
  hgvsp: ENSP00000389542.3:p.Pro1543Leu
  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.4124C>T
  hgvsp: ENSP00000386127.2:p.Pro1375Leu
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1516Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

9-73151448-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151448
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151448
    reference: chr 9
allele count: 3
allele frequency: 2.473533194815474e-5
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.4161T>C
  hgvsp: ENST00000377106.1:c.4161T>C(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.4626T>C
  hgvsp: ENST00000423814.3:c.4626T>C(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.4131T>C
  hgvsp: ENST00000360823.2:c.4131T>C(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.4161T>C
  hgvsp: ENST00000396292.4:c.4161T>C(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.4122T>C
  hgvsp: ENST00000377105.1:c.4122T>C(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.4545T>C
  hgvsp: ENST00000377110.3:c.4545T>C(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.4122T>C
  hgvsp: ENST00000408909.2:c.4122T>C(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.4131T>C
  hgvsp: ENST00000358082.3:c.4131T>C(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.4092T>C
  hgvsp: ENST00000396280.5:c.4092T>C(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.4122T>C
  hgvsp: ENST00000396285.1:c.4122T>C(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.4557T>C
  hgvsp: ENST00000357533.2:c.4557T>C(p.%3D)
  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.3955+590T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1515Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS

9-73151449-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151449
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151449
    reference: chr 9
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
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.4130C>T
  hgvsp: ENSP00000350791.3:p.Ala1377Val
  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.4160C>T
  hgvsp: ENSP00000379587.4:p.Ala1387Val
  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.4121C>T
  hgvsp: ENSP00000366309.1:p.Ala1374Val
  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.4091C>T
  hgvsp: ENSP00000379576.5:p.Ala1364Val
  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.4130C>T
  hgvsp: ENSP00000354066.2:p.Ala1377Val
  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.3955+589C>T
  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.4121C>T
  hgvsp: ENSP00000386127.2:p.Ala1374Val
  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.4121C>T
  hgvsp: ENSP00000379581.1:p.Ala1374Val
  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.4625C>T
  hgvsp: ENSP00000389542.3:p.Ala1542Val
  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.4556C>T
  hgvsp: ENSP00000350140.2:p.Ala1519Val
  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.4160C>T
  hgvsp: ENSP00000366310.1:p.Ala1387Val
  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.4544C>T
  hgvsp: ENSP00000366314.2:p.Ala1515Val
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1515Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-73151450-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151450
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151450
    reference: chr 9
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
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.4159G>T
  hgvsp: ENSP00000366310.1:p.Ala1387Ser
  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.4120G>T
  hgvsp: ENSP00000379581.1:p.Ala1374Ser
  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.4129G>T
  hgvsp: ENSP00000354066.2:p.Ala1377Ser
  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.3955+588G>T
  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.4624G>T
  hgvsp: ENSP00000389542.3:p.Ala1542Ser
  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.4129G>T
  hgvsp: ENSP00000350791.3:p.Ala1377Ser
  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.4543G>T
  hgvsp: ENSP00000366314.2:p.Ala1515Ser
  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.4120G>T
  hgvsp: ENSP00000366309.1:p.Ala1374Ser
  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.4159G>T
  hgvsp: ENSP00000379587.4:p.Ala1387Ser
  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.4090G>T
  hgvsp: ENSP00000379576.5:p.Ala1364Ser
  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.4120G>T
  hgvsp: ENSP00000386127.2:p.Ala1374Ser
  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.4555G>T
  hgvsp: ENSP00000350140.2:p.Ala1519Ser
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1515Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

9-73151460-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151460
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151460
    reference: chr 9
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.4110T>C
  hgvsp: ENST00000396285.1:c.4110T>C(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.4149T>C
  hgvsp: ENST00000377106.1:c.4149T>C(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.4119T>C
  hgvsp: ENST00000358082.3:c.4119T>C(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.4545T>C
  hgvsp: ENST00000357533.2:c.4545T>C(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.4149T>C
  hgvsp: ENST00000396292.4:c.4149T>C(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.4614T>C
  hgvsp: ENST00000423814.3:c.4614T>C(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.4110T>C
  hgvsp: ENST00000408909.2:c.4110T>C(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.4080T>C
  hgvsp: ENST00000396280.5:c.4080T>C(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.4533T>C
  hgvsp: ENST00000377110.3:c.4533T>C(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.4119T>C
  hgvsp: ENST00000360823.2:c.4119T>C(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.4110T>C
  hgvsp: ENST00000377105.1:c.4110T>C(p.%3D)
  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.3955+578T>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1511Leu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

9-73151462-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151462
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151462
    reference: chr 9
allele count: 2
allele frequency: 1.64923970049807e-5
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.4117C>G
  hgvsp: ENSP00000350791.3:p.Leu1373Val
  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.4078C>G
  hgvsp: ENSP00000379576.5:p.Leu1360Val
  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.4147C>G
  hgvsp: ENSP00000379587.4:p.Leu1383Val
  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.4147C>G
  hgvsp: ENSP00000366310.1:p.Leu1383Val
  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.4543C>G
  hgvsp: ENSP00000350140.2:p.Leu1515Val
  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.4612C>G
  hgvsp: ENSP00000389542.3:p.Leu1538Val
  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.4117C>G
  hgvsp: ENSP00000354066.2:p.Leu1373Val
  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.4108C>G
  hgvsp: ENSP00000386127.2:p.Leu1370Val
  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.4108C>G
  hgvsp: ENSP00000366309.1:p.Leu1370Val
  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.4108C>G
  hgvsp: ENSP00000379581.1:p.Leu1370Val
  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.3955+576C>G
  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.4531C>G
  hgvsp: ENSP00000366314.2:p.Leu1511Val
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1511Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

9-73151470-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151470
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151470
    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: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.4139C>T
  hgvsp: ENSP00000366310.1:p.Thr1380Ile
  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.4109C>T
  hgvsp: ENSP00000350791.3:p.Thr1370Ile
  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.4139C>T
  hgvsp: ENSP00000379587.4:p.Thr1380Ile
  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.4100C>T
  hgvsp: ENSP00000379581.1:p.Thr1367Ile
  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.4604C>T
  hgvsp: ENSP00000389542.3:p.Thr1535Ile
  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.4100C>T
  hgvsp: ENSP00000386127.2:p.Thr1367Ile
  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.4109C>T
  hgvsp: ENSP00000354066.2:p.Thr1370Ile
  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.3955+568C>T
  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.4535C>T
  hgvsp: ENSP00000350140.2:p.Thr1512Ile
  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.4100C>T
  hgvsp: ENSP00000366309.1:p.Thr1367Ile
  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.4523C>T
  hgvsp: ENSP00000366314.2:p.Thr1508Ile
  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.4070C>T
  hgvsp: ENSP00000379576.5:p.Thr1357Ile
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6736
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr1508Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

9-73151472-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151472
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151472
    reference: chr 9
allele count: 105
allele frequency: 8.659793814432989e-4
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.4602C>G
  hgvsp: ENST00000423814.3:c.4602C>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.4068C>G
  hgvsp: ENST00000396280.5:c.4068C>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.4098C>G
  hgvsp: ENST00000408909.2:c.4098C>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.4533C>G
  hgvsp: ENST00000357533.2:c.4533C>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.4098C>G
  hgvsp: ENST00000377105.1:c.4098C>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.4107C>G
  hgvsp: ENST00000358082.3:c.4107C>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.4107C>G
  hgvsp: ENST00000360823.2:c.4107C>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.4521C>G
  hgvsp: ENST00000377110.3:c.4521C>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.4137C>G
  hgvsp: ENST00000377106.1:c.4137C>G(p.%3D)
  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.3955+566C>G
  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.4098C>G
  hgvsp: ENST00000396285.1:c.4098C>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.4137C>G
  hgvsp: ENST00000396292.4:c.4137C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1507Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-73151474-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151474
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151474
    reference: chr 9
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.4600A>G
  hgvsp: ENSP00000389542.3:p.Thr1534Ala
  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.4096A>G
  hgvsp: ENSP00000379581.1:p.Thr1366Ala
  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.4105A>G
  hgvsp: ENSP00000354066.2:p.Thr1369Ala
  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.4096A>G
  hgvsp: ENSP00000366309.1:p.Thr1366Ala
  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.4105A>G
  hgvsp: ENSP00000350791.3:p.Thr1369Ala
  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.4135A>G
  hgvsp: ENSP00000379587.4:p.Thr1379Ala
  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.4519A>G
  hgvsp: ENSP00000366314.2:p.Thr1507Ala
  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.4531A>G
  hgvsp: ENSP00000350140.2:p.Thr1511Ala
  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.4135A>G
  hgvsp: ENSP00000366310.1:p.Thr1379Ala
  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.4096A>G
  hgvsp: ENSP00000386127.2:p.Thr1366Ala
  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.3955+564A>G
  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.4066A>G
  hgvsp: ENSP00000379576.5:p.Thr1356Ala
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6724
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1507Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

9-73151485-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151485
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151485
    reference: chr 9
allele count: 13
allele frequency: 1.072359520902762e-4
allele num: 121228
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.4055G>A
  hgvsp: ENSP00000379576.5:p.Arg1352His
  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.4094G>A
  hgvsp: ENSP00000354066.2:p.Arg1365His
  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.4508G>A
  hgvsp: ENSP00000366314.2:p.Arg1503His
  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.4085G>A
  hgvsp: ENSP00000379581.1:p.Arg1362His
  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.4124G>A
  hgvsp: ENSP00000366310.1:p.Arg1375His
  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.4124G>A
  hgvsp: ENSP00000379587.4:p.Arg1375His
  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.4085G>A
  hgvsp: ENSP00000386127.2:p.Arg1362His
  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.4085G>A
  hgvsp: ENSP00000366309.1:p.Arg1362His
  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.4589G>A
  hgvsp: ENSP00000389542.3:p.Arg1530His
  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.4094G>A
  hgvsp: ENSP00000350791.3:p.Arg1365His
  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.4520G>A
  hgvsp: ENSP00000350140.2:p.Arg1507His
  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.3955+553G>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4439
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1503His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

9-73151489-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151489
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151489
    reference: chr 9
allele count: 1
allele frequency: 8.266649031148734e-6
allele num: 120968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.4585A>G
  hgvsp: ENSP00000389542.3:p.Ser1529Gly
  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.4081A>G
  hgvsp: ENSP00000386127.2:p.Ser1361Gly
  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.4090A>G
  hgvsp: ENSP00000350791.3:p.Ser1364Gly
  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.3955+549A>G
  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.4504A>G
  hgvsp: ENSP00000366314.2:p.Ser1502Gly
  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.4120A>G
  hgvsp: ENSP00000366310.1:p.Ser1374Gly
  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.4516A>G
  hgvsp: ENSP00000350140.2:p.Ser1506Gly
  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.4090A>G
  hgvsp: ENSP00000354066.2:p.Ser1364Gly
  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.4081A>G
  hgvsp: ENSP00000379581.1:p.Ser1361Gly
  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.4081A>G
  hgvsp: ENSP00000366309.1:p.Ser1361Gly
  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.4120A>G
  hgvsp: ENSP00000379587.4:p.Ser1374Gly
  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.4051A>G
  hgvsp: ENSP00000379576.5:p.Ser1351Gly
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3909
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1502Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-73151491-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151491
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151491
    reference: chr 9
allele count: 12
allele frequency: 9.92835040458028e-5
allele num: 120866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.4583G>T
  hgvsp: ENSP00000389542.3:p.Ser1528Ile
  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.4502G>T
  hgvsp: ENSP00000366314.2:p.Ser1501Ile
  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.4079G>T
  hgvsp: ENSP00000386127.2:p.Ser1360Ile
  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.4514G>T
  hgvsp: ENSP00000350140.2:p.Ser1505Ile
  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.4118G>T
  hgvsp: ENSP00000366310.1:p.Ser1373Ile
  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.4088G>T
  hgvsp: ENSP00000354066.2:p.Ser1363Ile
  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.3955+547G>T
  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.4079G>T
  hgvsp: ENSP00000379581.1:p.Ser1360Ile
  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.4088G>T
  hgvsp: ENSP00000350791.3:p.Ser1363Ile
  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.4079G>T
  hgvsp: ENSP00000366309.1:p.Ser1360Ile
  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.4118G>T
  hgvsp: ENSP00000379587.4:p.Ser1373Ile
  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.4049G>T
  hgvsp: ENSP00000379576.5:p.Ser1350Ile
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 6866
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1501Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

9-73151496-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151496
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151496
    reference: chr 9
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.4509C>A
  hgvsp: ENST00000357533.2:c.4509C>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.4113C>A
  hgvsp: ENST00000377106.1:c.4113C>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.4074C>A
  hgvsp: ENST00000396285.1:c.4074C>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.4083C>A
  hgvsp: ENST00000358082.3:c.4083C>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.4497C>A
  hgvsp: ENST00000377110.3:c.4497C>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.4044C>A
  hgvsp: ENST00000396280.5:c.4044C>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.4113C>A
  hgvsp: ENST00000396292.4:c.4113C>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.4578C>A
  hgvsp: ENST00000423814.3:c.4578C>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.4083C>A
  hgvsp: ENST00000360823.2:c.4083C>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.4074C>A
  hgvsp: ENST00000377105.1:c.4074C>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.4074C>A
  hgvsp: ENST00000408909.2:c.4074C>A(p.%3D)
  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.3955+542C>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1499Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

9-73151497-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151497
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151497
    reference: chr 9
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.4073C>T
  hgvsp: ENSP00000386127.2:p.Ser1358Phe
  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.4577C>T
  hgvsp: ENSP00000389542.3:p.Ser1526Phe
  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.4082C>T
  hgvsp: ENSP00000350791.3:p.Ser1361Phe
  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.4112C>T
  hgvsp: ENSP00000366310.1:p.Ser1371Phe
  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.4082C>T
  hgvsp: ENSP00000354066.2:p.Ser1361Phe
  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.4112C>T
  hgvsp: ENSP00000379587.4:p.Ser1371Phe
  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.3955+541C>T
  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.4073C>T
  hgvsp: ENSP00000379581.1:p.Ser1358Phe
  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.4073C>T
  hgvsp: ENSP00000366309.1:p.Ser1358Phe
  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.4043C>T
  hgvsp: ENSP00000379576.5:p.Ser1348Phe
  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.4496C>T
  hgvsp: ENSP00000366314.2:p.Ser1499Phe
  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.4508C>T
  hgvsp: ENSP00000350140.2:p.Ser1503Phe
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1499Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

9-73151500-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151500
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151500
    reference: chr 9
allele count: 5
allele frequency: 4.125616779708567e-5
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.4079G>A
  hgvsp: ENSP00000350791.3:p.Arg1360His
  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.4070G>A
  hgvsp: ENSP00000379581.1:p.Arg1357His
  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.4505G>A
  hgvsp: ENSP00000350140.2:p.Arg1502His
  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.4574G>A
  hgvsp: ENSP00000389542.3:p.Arg1525His
  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.4079G>A
  hgvsp: ENSP00000354066.2:p.Arg1360His
  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.4493G>A
  hgvsp: ENSP00000366314.2:p.Arg1498His
  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.4040G>A
  hgvsp: ENSP00000379576.5:p.Arg1347His
  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.4070G>A
  hgvsp: ENSP00000386127.2:p.Arg1357His
  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.4070G>A
  hgvsp: ENSP00000366309.1:p.Arg1357His
  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.4109G>A
  hgvsp: ENSP00000366310.1:p.Arg1370His
  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.4109G>A
  hgvsp: ENSP00000379587.4:p.Arg1370His
  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.3955+538G>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4581
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1498His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

9-73151503-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151503
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151503
    reference: chr 9
allele count: 3
allele frequency: 2.474553343121567e-5
allele num: 121234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.4106A>T
  hgvsp: ENSP00000379587.4:p.Glu1369Val
  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.4037A>T
  hgvsp: ENSP00000379576.5:p.Glu1346Val
  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.4067A>T
  hgvsp: ENSP00000379581.1:p.Glu1356Val
  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.3955+535A>T
  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.4571A>T
  hgvsp: ENSP00000389542.3:p.Glu1524Val
  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.4502A>T
  hgvsp: ENSP00000350140.2:p.Glu1501Val
  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.4076A>T
  hgvsp: ENSP00000350791.3:p.Glu1359Val
  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.4106A>T
  hgvsp: ENSP00000366310.1:p.Glu1369Val
  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.4076A>T
  hgvsp: ENSP00000354066.2:p.Glu1359Val
  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.4067A>T
  hgvsp: ENSP00000366309.1:p.Glu1356Val
  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.4067A>T
  hgvsp: ENSP00000386127.2:p.Glu1356Val
  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.4490A>T
  hgvsp: ENSP00000366314.2:p.Glu1497Val
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3910
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1497Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

9-73151505-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151505
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151505
    reference: chr 9
allele count: 2
allele frequency: 1.649484536082474e-5
allele num: 121250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.4065T>C
  hgvsp: ENST00000396285.1:c.4065T>C(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.4065T>C
  hgvsp: ENST00000377105.1:c.4065T>C(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.4074T>C
  hgvsp: ENST00000358082.3:c.4074T>C(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.4074T>C
  hgvsp: ENST00000360823.2:c.4074T>C(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.4104T>C
  hgvsp: ENST00000396292.4:c.4104T>C(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.4065T>C
  hgvsp: ENST00000408909.2:c.4065T>C(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.4488T>C
  hgvsp: ENST00000377110.3:c.4488T>C(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.4104T>C
  hgvsp: ENST00000377106.1:c.4104T>C(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.4569T>C
  hgvsp: ENST00000423814.3:c.4569T>C(p.%3D)
  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.3955+533T>C
  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.4035T>C
  hgvsp: ENST00000396280.5:c.4035T>C(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.4500T>C
  hgvsp: ENST00000357533.2:c.4500T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3911
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1496Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

9-73151506-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151506
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151506
    reference: chr 9
allele count: 2
allele frequency: 1.649484536082474e-5
allele num: 121250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.4064T>C
  hgvsp: ENSP00000379581.1:p.Ile1355Thr
  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.4568T>C
  hgvsp: ENSP00000389542.3:p.Ile1523Thr
  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.4103T>C
  hgvsp: ENSP00000366310.1:p.Ile1368Thr
  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.4487T>C
  hgvsp: ENSP00000366314.2:p.Ile1496Thr
  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.4034T>C
  hgvsp: ENSP00000379576.5:p.Ile1345Thr
  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.4103T>C
  hgvsp: ENSP00000379587.4:p.Ile1368Thr
  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.4073T>C
  hgvsp: ENSP00000350791.3:p.Ile1358Thr
  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.4073T>C
  hgvsp: ENSP00000354066.2:p.Ile1358Thr
  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.4064T>C
  hgvsp: ENSP00000366309.1:p.Ile1355Thr
  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.3955+532T>C
  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.4499T>C
  hgvsp: ENSP00000350140.2:p.Ile1500Thr
  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.4064T>C
  hgvsp: ENSP00000386127.2:p.Ile1355Thr
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3912
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile1496Thr
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS

9-73151520-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151520
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151520
    reference: chr 9
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.4050G>C
  hgvsp: ENST00000408909.2:c.4050G>C(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.4059G>C
  hgvsp: ENST00000358082.3:c.4059G>C(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.4050G>C
  hgvsp: ENST00000396285.1:c.4050G>C(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.4089G>C
  hgvsp: ENST00000377106.1:c.4089G>C(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.4554G>C
  hgvsp: ENST00000423814.3:c.4554G>C(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.4485G>C
  hgvsp: ENST00000357533.2:c.4485G>C(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.4020G>C
  hgvsp: ENST00000396280.5:c.4020G>C(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.4059G>C
  hgvsp: ENST00000360823.2:c.4059G>C(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.4473G>C
  hgvsp: ENST00000377110.3:c.4473G>C(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.4089G>C
  hgvsp: ENST00000396292.4:c.4089G>C(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.4050G>C
  hgvsp: ENST00000377105.1:c.4050G>C(p.%3D)
  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.3955+518G>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1491Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

9-73151520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151520
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151520
    reference: chr 9
allele count: 3
allele frequency: 2.474798303938229e-5
allele num: 121222
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.4020G>A
  hgvsp: ENST00000396280.5:c.4020G>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.4059G>A
  hgvsp: ENST00000360823.2:c.4059G>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.4554G>A
  hgvsp: ENST00000423814.3:c.4554G>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.4059G>A
  hgvsp: ENST00000358082.3:c.4059G>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.4485G>A
  hgvsp: ENST00000357533.2:c.4485G>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.4050G>A
  hgvsp: ENST00000408909.2:c.4050G>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.4473G>A
  hgvsp: ENST00000377110.3:c.4473G>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.4089G>A
  hgvsp: ENST00000396292.4:c.4089G>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.4050G>A
  hgvsp: ENST00000396285.1:c.4050G>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.4089G>A
  hgvsp: ENST00000377106.1:c.4089G>A(p.%3D)
  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.3955+518G>A
  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.4050G>A
  hgvsp: ENST00000377105.1:c.4050G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1491Pro
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

9-73151521-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151521
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151521
    reference: chr 9
allele count: 4
allele frequency: 3.298969072164949e-5
allele num: 121250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.4088C>T
  hgvsp: ENSP00000379587.4:p.Pro1363Leu
  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.4058C>T
  hgvsp: ENSP00000350791.3:p.Pro1353Leu
  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.4019C>T
  hgvsp: ENSP00000379576.5:p.Pro1340Leu
  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.4472C>T
  hgvsp: ENSP00000366314.2:p.Pro1491Leu
  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.4484C>T
  hgvsp: ENSP00000350140.2:p.Pro1495Leu
  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.4058C>T
  hgvsp: ENSP00000354066.2:p.Pro1353Leu
  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.3955+517C>T
  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.4049C>T
  hgvsp: ENSP00000366309.1:p.Pro1350Leu
  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.4088C>T
  hgvsp: ENSP00000366310.1:p.Pro1363Leu
  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.4553C>T
  hgvsp: ENSP00000389542.3:p.Pro1518Leu
  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.4049C>T
  hgvsp: ENSP00000379581.1:p.Pro1350Leu
  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.4049C>T
  hgvsp: ENSP00000386127.2:p.Pro1350Leu
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1491Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

9-73151548-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151548
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151548
    reference: chr 9
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366310
  ensembl transcript: ENST00000377106
  gene symbol: TRPM3
  hgvsc: ENST00000377106.1:c.4061G>A
  hgvsp: ENSP00000366310.1:p.Cys1354Tyr
  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.4031G>A
  hgvsp: ENSP00000354066.2:p.Cys1344Tyr
  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.4022G>A
  hgvsp: ENSP00000379581.1:p.Cys1341Tyr
  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.4061G>A
  hgvsp: ENSP00000379587.4:p.Cys1354Tyr
  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.3992G>A
  hgvsp: ENSP00000379576.5:p.Cys1331Tyr
  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.4457G>A
  hgvsp: ENSP00000350140.2:p.Cys1486Tyr
  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.4031G>A
  hgvsp: ENSP00000350791.3:p.Cys1344Tyr
  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.3955+490G>A
  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.4526G>A
  hgvsp: ENSP00000389542.3:p.Cys1509Tyr
  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.4022G>A
  hgvsp: ENSP00000366309.1:p.Cys1341Tyr
  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.4022G>A
  hgvsp: ENSP00000386127.2:p.Cys1341Tyr
  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.4445G>A
  hgvsp: ENSP00000366314.2:p.Cys1482Tyr
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys1482Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-73151549-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151549
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151549
    reference: chr 9
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.4021T>C
  hgvsp: ENSP00000386127.2:p.Cys1341Arg
  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.4030T>C
  hgvsp: ENSP00000350791.3:p.Cys1344Arg
  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.4021T>C
  hgvsp: ENSP00000379581.1:p.Cys1341Arg
  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.4456T>C
  hgvsp: ENSP00000350140.2:p.Cys1486Arg
  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.3955+489T>C
  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.4060T>C
  hgvsp: ENSP00000366310.1:p.Cys1354Arg
  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.3991T>C
  hgvsp: ENSP00000379576.5:p.Cys1331Arg
  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.4444T>C
  hgvsp: ENSP00000366314.2:p.Cys1482Arg
  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.4021T>C
  hgvsp: ENSP00000366309.1:p.Cys1341Arg
  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.4030T>C
  hgvsp: ENSP00000354066.2:p.Cys1344Arg
  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.4525T>C
  hgvsp: ENSP00000389542.3:p.Cys1509Arg
  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.4060T>C
  hgvsp: ENSP00000379587.4:p.Cys1354Arg
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Cys1482Arg
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

9-73151552-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151552
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151552
    reference: chr 9
allele count: 53
allele frequency: 4.368467904124493e-4
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.4453G>C
  hgvsp: ENSP00000350140.2:p.Glu1485Gln
  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.4057G>C
  hgvsp: ENSP00000366310.1:p.Glu1353Gln
  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.3988G>C
  hgvsp: ENSP00000379576.5:p.Glu1330Gln
  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.4057G>C
  hgvsp: ENSP00000379587.4:p.Glu1353Gln
  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.4441G>C
  hgvsp: ENSP00000366314.2:p.Glu1481Gln
  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.4018G>C
  hgvsp: ENSP00000379581.1:p.Glu1340Gln
  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.4027G>C
  hgvsp: ENSP00000354066.2:p.Glu1343Gln
  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.4522G>C
  hgvsp: ENSP00000389542.3:p.Glu1508Gln
  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.4018G>C
  hgvsp: ENSP00000366309.1:p.Glu1340Gln
  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.4018G>C
  hgvsp: ENSP00000386127.2:p.Glu1340Gln
  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.3955+486G>C
  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.4027G>C
  hgvsp: ENSP00000350791.3:p.Glu1343Gln
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Glu1481Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS

9-73151552-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151552
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151552
    reference: chr 9
allele count: 6
allele frequency: 4.945435363159804e-5
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.4057G>A
  hgvsp: ENSP00000379587.4:p.Glu1353Lys
  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.3955+486G>A
  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.4522G>A
  hgvsp: ENSP00000389542.3:p.Glu1508Lys
  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.4018G>A
  hgvsp: ENSP00000386127.2:p.Glu1340Lys
  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.4057G>A
  hgvsp: ENSP00000366310.1:p.Glu1353Lys
  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.4018G>A
  hgvsp: ENSP00000379581.1:p.Glu1340Lys
  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.4027G>A
  hgvsp: ENSP00000350791.3:p.Glu1343Lys
  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.4441G>A
  hgvsp: ENSP00000366314.2:p.Glu1481Lys
  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.4453G>A
  hgvsp: ENSP00000350140.2:p.Glu1485Lys
  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.4027G>A
  hgvsp: ENSP00000354066.2:p.Glu1343Lys
  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.3988G>A
  hgvsp: ENSP00000379576.5:p.Glu1330Lys
  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.4018G>A
  hgvsp: ENSP00000366309.1:p.Glu1340Lys
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu1481Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

9-73151553-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151553
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151553
    reference: chr 9
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.4017A>G
  hgvsp: ENST00000408909.2:c.4017A>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.4056A>G
  hgvsp: ENST00000396292.4:c.4056A>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.4452A>G
  hgvsp: ENST00000357533.2:c.4452A>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.4026A>G
  hgvsp: ENST00000360823.2:c.4026A>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.4017A>G
  hgvsp: ENST00000396285.1:c.4017A>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.3987A>G
  hgvsp: ENST00000396280.5:c.3987A>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.4026A>G
  hgvsp: ENST00000358082.3:c.4026A>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.4056A>G
  hgvsp: ENST00000377106.1:c.4056A>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.4521A>G
  hgvsp: ENST00000423814.3:c.4521A>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.4017A>G
  hgvsp: ENST00000377105.1:c.4017A>G(p.%3D)
  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.3955+485A>G
  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.4440A>G
  hgvsp: ENST00000377110.3:c.4440A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1480Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

9-73151569-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151569
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151569
    reference: chr 9
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.4010A>G
  hgvsp: ENSP00000354066.2:p.Asp1337Gly
  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.3971A>G
  hgvsp: ENSP00000379576.5:p.Asp1324Gly
  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.4040A>G
  hgvsp: ENSP00000379587.4:p.Asp1347Gly
  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.4436A>G
  hgvsp: ENSP00000350140.2:p.Asp1479Gly
  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.4010A>G
  hgvsp: ENSP00000350791.3:p.Asp1337Gly
  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.4040A>G
  hgvsp: ENSP00000366310.1:p.Asp1347Gly
  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.4001A>G
  hgvsp: ENSP00000386127.2:p.Asp1334Gly
  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.4001A>G
  hgvsp: ENSP00000366309.1:p.Asp1334Gly
  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.4001A>G
  hgvsp: ENSP00000379581.1:p.Asp1334Gly
  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.4505A>G
  hgvsp: ENSP00000389542.3:p.Asp1502Gly
  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.3955+469A>G
  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.4424A>G
  hgvsp: ENSP00000366314.2:p.Asp1475Gly
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp1475Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/9-73151570-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151570
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151570
    reference: chr 9
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366309
  ensembl transcript: ENST00000377105
  gene symbol: TRPM3
  hgvsc: ENST00000377105.1:c.4000G>T
  hgvsp: ENSP00000366309.1:p.Asp1334Tyr
  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.4423G>T
  hgvsp: ENSP00000366314.2:p.Asp1475Tyr
  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.4000G>T
  hgvsp: ENSP00000379581.1:p.Asp1334Tyr
  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.4435G>T
  hgvsp: ENSP00000350140.2:p.Asp1479Tyr
  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.4039G>T
  hgvsp: ENSP00000379587.4:p.Asp1347Tyr
  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.4009G>T
  hgvsp: ENSP00000350791.3:p.Asp1337Tyr
  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.4039G>T
  hgvsp: ENSP00000366310.1:p.Asp1347Tyr
  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.4009G>T
  hgvsp: ENSP00000354066.2:p.Asp1337Tyr
  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.4000G>T
  hgvsp: ENSP00000386127.2:p.Asp1334Tyr
  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.3955+468G>T
  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.3970G>T
  hgvsp: ENSP00000379576.5:p.Asp1324Tyr
  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.4504G>T
  hgvsp: ENSP00000389542.3:p.Asp1502Tyr
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp1475Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-73151588-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151588
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151588
    reference: chr 9
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.3982A>T
  hgvsp: ENSP00000379581.1:p.Thr1328Ser
  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.3952A>T
  hgvsp: ENSP00000379576.5:p.Thr1318Ser
  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.4417A>T
  hgvsp: ENSP00000350140.2:p.Thr1473Ser
  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.4486A>T
  hgvsp: ENSP00000389542.3:p.Thr1496Ser
  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.4405A>T
  hgvsp: ENSP00000366314.2:p.Thr1469Ser
  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.4021A>T
  hgvsp: ENSP00000379587.4:p.Thr1341Ser
  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.4021A>T
  hgvsp: ENSP00000366310.1:p.Thr1341Ser
  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.3991A>T
  hgvsp: ENSP00000350791.3:p.Thr1331Ser
  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.3955+450A>T
  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.3991A>T
  hgvsp: ENSP00000354066.2:p.Thr1331Ser
  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.3982A>T
  hgvsp: ENSP00000386127.2:p.Thr1328Ser
  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.3982A>T
  hgvsp: ENSP00000366309.1:p.Thr1328Ser
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1469Ser
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

9-73151589-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151589
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151589
    reference: chr 9
allele count: 53
allele frequency: 4.365876964644634e-4
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.3955+449C>T
  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.3981C>T
  hgvsp: ENST00000396285.1:c.3981C>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.3981C>T
  hgvsp: ENST00000408909.2:c.3981C>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.4416C>T
  hgvsp: ENST00000357533.2:c.4416C>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.4020C>T
  hgvsp: ENST00000396292.4:c.4020C>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.3951C>T
  hgvsp: ENST00000396280.5:c.3951C>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.3990C>T
  hgvsp: ENST00000360823.2:c.3990C>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.4020C>T
  hgvsp: ENST00000377106.1:c.4020C>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.3990C>T
  hgvsp: ENST00000358082.3:c.3990C>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.4485C>T
  hgvsp: ENST00000423814.3:c.4485C>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.4404C>T
  hgvsp: ENST00000377110.3:c.4404C>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.3981C>T
  hgvsp: ENST00000377105.1:c.3981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2154
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Asp1468Asp
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

9-73151601-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151601
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151601
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379581
  ensembl transcript: ENST00000396285
  gene symbol: TRPM3
  hgvsc: ENST00000396285.1:c.3969C>T
  hgvsp: ENST00000396285.1:c.3969C>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.4008C>T
  hgvsp: ENST00000396292.4:c.4008C>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.4392C>T
  hgvsp: ENST00000377110.3:c.4392C>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.3978C>T
  hgvsp: ENST00000360823.2:c.3978C>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.3939C>T
  hgvsp: ENST00000396280.5:c.3939C>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.4473C>T
  hgvsp: ENST00000423814.3:c.4473C>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.4008C>T
  hgvsp: ENST00000377106.1:c.4008C>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.3978C>T
  hgvsp: ENST00000358082.3:c.3978C>T(p.%3D)
  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.3955+437C>T
  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.3969C>T
  hgvsp: ENST00000377105.1:c.3969C>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.4404C>T
  hgvsp: ENST00000357533.2:c.4404C>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.3969C>T
  hgvsp: ENST00000408909.2:c.3969C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6831
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1464Ile
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

9-73151615-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151615
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151615
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
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.3925G>A
  hgvsp: ENSP00000379576.5:p.Asp1309Asn
  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.3994G>A
  hgvsp: ENSP00000379587.4:p.Asp1332Asn
  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.4390G>A
  hgvsp: ENSP00000350140.2:p.Asp1464Asn
  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.3955G>A
  hgvsp: ENSP00000386127.2:p.Asp1319Asn
  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.3994G>A
  hgvsp: ENSP00000366310.1:p.Asp1332Asn
  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.3964G>A
  hgvsp: ENSP00000350791.3:p.Asp1322Asn
  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.3955G>A
  hgvsp: ENSP00000366309.1:p.Asp1319Asn
  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.3955G>A
  hgvsp: ENSP00000379581.1:p.Asp1319Asn
  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.3964G>A
  hgvsp: ENSP00000354066.2:p.Asp1322Asn
  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.4459G>A
  hgvsp: ENSP00000389542.3:p.Asp1487Asn
  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.4378G>A
  hgvsp: ENSP00000366314.2:p.Asp1460Asn
  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.3955+423G>A
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6831
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2842
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp1460Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum

9-73151617-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151617
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151617
    reference: chr 9
allele count: 4
allele frequency: 3.294730079238259e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.3962T>C
  hgvsp: ENSP00000350791.3:p.Ile1321Thr
  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.3955+421T>C
  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.3953T>C
  hgvsp: ENSP00000379581.1:p.Ile1318Thr
  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.3923T>C
  hgvsp: ENSP00000379576.5:p.Ile1308Thr
  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.3962T>C
  hgvsp: ENSP00000354066.2:p.Ile1321Thr
  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.4457T>C
  hgvsp: ENSP00000389542.3:p.Ile1486Thr
  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.3953T>C
  hgvsp: ENSP00000386127.2:p.Ile1318Thr
  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.3992T>C
  hgvsp: ENSP00000366310.1:p.Ile1331Thr
  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.3992T>C
  hgvsp: ENSP00000379587.4:p.Ile1331Thr
  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.4388T>C
  hgvsp: ENSP00000350140.2:p.Ile1463Thr
  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.3953T>C
  hgvsp: ENSP00000366309.1:p.Ile1318Thr
  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.4376T>C
  hgvsp: ENSP00000366314.2:p.Ile1459Thr
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1459Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

9-73151618-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151618
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151618
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.3961A>G
  hgvsp: ENSP00000354066.2:p.Ile1321Val
  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.3991A>G
  hgvsp: ENSP00000366310.1:p.Ile1331Val
  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.4375A>G
  hgvsp: ENSP00000366314.2:p.Ile1459Val
  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.3952A>G
  hgvsp: ENSP00000379581.1:p.Ile1318Val
  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.3961A>G
  hgvsp: ENSP00000350791.3:p.Ile1321Val
  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.4456A>G
  hgvsp: ENSP00000389542.3:p.Ile1486Val
  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.3952A>G
  hgvsp: ENSP00000386127.2:p.Ile1318Val
  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.3922A>G
  hgvsp: ENSP00000379576.5:p.Ile1308Val
  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.4387A>G
  hgvsp: ENSP00000350140.2:p.Ile1463Val
  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.3955+420A>G
  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.3991A>G
  hgvsp: ENSP00000379587.4:p.Ile1331Val
  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.3952A>G
  hgvsp: ENSP00000366309.1:p.Ile1318Val
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile1459Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-73151623-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151623
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151623
    reference: chr 9
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.3956G>T
  hgvsp: ENSP00000354066.2:p.Arg1319Leu
  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.4370G>T
  hgvsp: ENSP00000366314.2:p.Arg1457Leu
  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.3986G>T
  hgvsp: ENSP00000379587.4:p.Arg1329Leu
  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.4451G>T
  hgvsp: ENSP00000389542.3:p.Arg1484Leu
  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.3917G>T
  hgvsp: ENSP00000379576.5:p.Arg1306Leu
  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.3947G>T
  hgvsp: ENSP00000386127.2:p.Arg1316Leu
  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.4382G>T
  hgvsp: ENSP00000350140.2:p.Arg1461Leu
  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.3986G>T
  hgvsp: ENSP00000366310.1:p.Arg1329Leu
  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.3956G>T
  hgvsp: ENSP00000350791.3:p.Arg1319Leu
  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.3947G>T
  hgvsp: ENSP00000379581.1:p.Arg1316Leu
  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.3955+415G>T
  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.3947G>T
  hgvsp: ENSP00000366309.1:p.Arg1316Leu
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1457Leu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

9-73151623-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151623
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151623
    reference: chr 9
allele count: 6
allele frequency: 4.942095118857387e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.3986G>A
  hgvsp: ENSP00000379587.4:p.Arg1329Gln
  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.4382G>A
  hgvsp: ENSP00000350140.2:p.Arg1461Gln
  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.3986G>A
  hgvsp: ENSP00000366310.1:p.Arg1329Gln
  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.3917G>A
  hgvsp: ENSP00000379576.5:p.Arg1306Gln
  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.3947G>A
  hgvsp: ENSP00000366309.1:p.Arg1316Gln
  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.3947G>A
  hgvsp: ENSP00000379581.1:p.Arg1316Gln
  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.3956G>A
  hgvsp: ENSP00000354066.2:p.Arg1319Gln
  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.3955+415G>A
  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.4370G>A
  hgvsp: ENSP00000366314.2:p.Arg1457Gln
  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.4451G>A
  hgvsp: ENSP00000389542.3:p.Arg1484Gln
  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.3956G>A
  hgvsp: ENSP00000350791.3:p.Arg1319Gln
  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.3947G>A
  hgvsp: ENSP00000386127.2:p.Arg1316Gln
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1457Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

9-73151625-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151625
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151625
    reference: chr 9
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.3984C>A
  hgvsp: ENSP00000379587.4:p.Ser1328Arg
  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.3984C>A
  hgvsp: ENSP00000366310.1:p.Ser1328Arg
  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.4449C>A
  hgvsp: ENSP00000389542.3:p.Ser1483Arg
  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.3954C>A
  hgvsp: ENSP00000354066.2:p.Ser1318Arg
  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.3945C>A
  hgvsp: ENSP00000366309.1:p.Ser1315Arg
  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.3945C>A
  hgvsp: ENSP00000379581.1:p.Ser1315Arg
  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.3955+413C>A
  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.3915C>A
  hgvsp: ENSP00000379576.5:p.Ser1305Arg
  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.3945C>A
  hgvsp: ENSP00000386127.2:p.Ser1315Arg
  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.4368C>A
  hgvsp: ENSP00000366314.2:p.Ser1456Arg
  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.3954C>A
  hgvsp: ENSP00000350791.3:p.Ser1318Arg
  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.4380C>A
  hgvsp: ENSP00000350140.2:p.Ser1460Arg
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1456Arg
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

9-73151626-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151626
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151626
    reference: chr 9
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
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.3953G>A
  hgvsp: ENSP00000354066.2:p.Ser1318Asn
  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.4448G>A
  hgvsp: ENSP00000389542.3:p.Ser1483Asn
  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.3955+412G>A
  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.3983G>A
  hgvsp: ENSP00000379587.4:p.Ser1328Asn
  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.3944G>A
  hgvsp: ENSP00000386127.2:p.Ser1315Asn
  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.4367G>A
  hgvsp: ENSP00000366314.2:p.Ser1456Asn
  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.3944G>A
  hgvsp: ENSP00000379581.1:p.Ser1315Asn
  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.3983G>A
  hgvsp: ENSP00000366310.1:p.Ser1328Asn
  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.3914G>A
  hgvsp: ENSP00000379576.5:p.Ser1305Asn
  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.3953G>A
  hgvsp: ENSP00000350791.3:p.Ser1318Asn
  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.4379G>A
  hgvsp: ENSP00000350140.2:p.Ser1460Asn
  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.3944G>A
  hgvsp: ENSP00000366309.1:p.Ser1315Asn
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1456Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

9-73151633-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151633
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151633
    reference: chr 9
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
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.3976C>T
  hgvsp: ENSP00000366310.1:p.Pro1326Ser
  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.3946C>T
  hgvsp: ENSP00000354066.2:p.Pro1316Ser
  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.3946C>T
  hgvsp: ENSP00000350791.3:p.Pro1316Ser
  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.3937C>T
  hgvsp: ENSP00000386127.2:p.Pro1313Ser
  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.3907C>T
  hgvsp: ENSP00000379576.5:p.Pro1303Ser
  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.3976C>T
  hgvsp: ENSP00000379587.4:p.Pro1326Ser
  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.3955+405C>T
  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.4441C>T
  hgvsp: ENSP00000389542.3:p.Pro1481Ser
  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.3937C>T
  hgvsp: ENSP00000366309.1:p.Pro1313Ser
  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.3937C>T
  hgvsp: ENSP00000379581.1:p.Pro1313Ser
  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.4372C>T
  hgvsp: ENSP00000350140.2:p.Pro1458Ser
  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.4360C>T
  hgvsp: ENSP00000366314.2:p.Pro1454Ser
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6831
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1454Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

9-73151637-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151637
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151637
    reference: chr 9
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366314
  ensembl transcript: ENST00000377110
  gene symbol: TRPM3
  hgvsc: ENST00000377110.3:c.4356C>T
  hgvsp: ENST00000377110.3:c.4356C>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.3942C>T
  hgvsp: ENST00000360823.2:c.3942C>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.4368C>T
  hgvsp: ENST00000357533.2:c.4368C>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.3933C>T
  hgvsp: ENST00000396285.1:c.3933C>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.3972C>T
  hgvsp: ENST00000396292.4:c.3972C>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.4437C>T
  hgvsp: ENST00000423814.3:c.4437C>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.3933C>T
  hgvsp: ENST00000408909.2:c.3933C>T(p.%3D)
  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.3955+401C>T
  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.3942C>T
  hgvsp: ENST00000358082.3:c.3942C>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.3903C>T
  hgvsp: ENST00000396280.5:c.3903C>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.3933C>T
  hgvsp: ENST00000377105.1:c.3933C>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.3972C>T
  hgvsp: ENST00000377106.1:c.3972C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp1452Asp
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

9-73151638-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151638
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151638
    reference: chr 9
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379576
  ensembl transcript: ENST00000396280
  gene symbol: TRPM3
  hgvsc: ENST00000396280.5:c.3902A>G
  hgvsp: ENSP00000379576.5:p.Asp1301Gly
  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.3971A>G
  hgvsp: ENSP00000366310.1:p.Asp1324Gly
  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.3941A>G
  hgvsp: ENSP00000354066.2:p.Asp1314Gly
  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.3955+400A>G
  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.4355A>G
  hgvsp: ENSP00000366314.2:p.Asp1452Gly
  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.3932A>G
  hgvsp: ENSP00000386127.2:p.Asp1311Gly
  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.4436A>G
  hgvsp: ENSP00000389542.3:p.Asp1479Gly
  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.3971A>G
  hgvsp: ENSP00000379587.4:p.Asp1324Gly
  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.4367A>G
  hgvsp: ENSP00000350140.2:p.Asp1456Gly
  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.3932A>G
  hgvsp: ENSP00000379581.1:p.Asp1311Gly
  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.3941A>G
  hgvsp: ENSP00000350791.3:p.Asp1314Gly
  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.3932A>G
  hgvsp: ENSP00000366309.1:p.Asp1311Gly
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5059
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp1452Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

9-73151653-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151653
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151653
    reference: chr 9
allele count: 5
allele frequency: 4.118276912939626e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350791
  ensembl transcript: ENST00000358082
  gene symbol: TRPM3
  hgvsc: ENST00000358082.3:c.3926C>A
  hgvsp: ENSP00000350791.3:p.Thr1309Lys
  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.3955+385C>A
  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.3926C>A
  hgvsp: ENSP00000354066.2:p.Thr1309Lys
  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.4340C>A
  hgvsp: ENSP00000366314.2:p.Thr1447Lys
  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.3917C>A
  hgvsp: ENSP00000386127.2:p.Thr1306Lys
  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.3956C>A
  hgvsp: ENSP00000366310.1:p.Thr1319Lys
  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.3917C>A
  hgvsp: ENSP00000366309.1:p.Thr1306Lys
  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.4352C>A
  hgvsp: ENSP00000350140.2:p.Thr1451Lys
  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.3956C>A
  hgvsp: ENSP00000379587.4:p.Thr1319Lys
  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.3917C>A
  hgvsp: ENSP00000379581.1:p.Thr1306Lys
  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.3887C>A
  hgvsp: ENSP00000379576.5:p.Thr1296Lys
  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.4421C>A
  hgvsp: ENSP00000389542.3:p.Thr1474Lys
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6835
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1447Lys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

9-73151659-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151659
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151659
    reference: chr 9
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
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.3920A>T
  hgvsp: ENSP00000350791.3:p.Tyr1307Phe
  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.3950A>T
  hgvsp: ENSP00000379587.4:p.Tyr1317Phe
  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.3911A>T
  hgvsp: ENSP00000386127.2:p.Tyr1304Phe
  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.4415A>T
  hgvsp: ENSP00000389542.3:p.Tyr1472Phe
  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.3911A>T
  hgvsp: ENSP00000379581.1:p.Tyr1304Phe
  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.4346A>T
  hgvsp: ENSP00000350140.2:p.Tyr1449Phe
  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.3911A>T
  hgvsp: ENSP00000366309.1:p.Tyr1304Phe
  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.4334A>T
  hgvsp: ENSP00000366314.2:p.Tyr1445Phe
  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.3955+379A>T
  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.3881A>T
  hgvsp: ENSP00000379576.5:p.Tyr1294Phe
  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.3920A>T
  hgvsp: ENSP00000354066.2:p.Tyr1307Phe
  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.3950A>T
  hgvsp: ENSP00000366310.1:p.Tyr1317Phe
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr1445Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

9-73151660-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151660
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151660
    reference: chr 9
allele count: 6
allele frequency: 4.942013705851344e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.3919T>C
  hgvsp: ENSP00000354066.2:p.Tyr1307His
  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.4333T>C
  hgvsp: ENSP00000366314.2:p.Tyr1445His
  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.3949T>C
  hgvsp: ENSP00000379587.4:p.Tyr1317His
  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.3949T>C
  hgvsp: ENSP00000366310.1:p.Tyr1317His
  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.3955+378T>C
  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.3919T>C
  hgvsp: ENSP00000350791.3:p.Tyr1307His
  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.3910T>C
  hgvsp: ENSP00000379581.1:p.Tyr1304His
  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.3910T>C
  hgvsp: ENSP00000366309.1:p.Tyr1304His
  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.4414T>C
  hgvsp: ENSP00000389542.3:p.Tyr1472His
  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.3910T>C
  hgvsp: ENSP00000386127.2:p.Tyr1304His
  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.4345T>C
  hgvsp: ENSP00000350140.2:p.Tyr1449His
  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.3880T>C
  hgvsp: ENSP00000379576.5:p.Tyr1294His
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr1445His
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-73151662-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151662
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151662
    reference: chr 9
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
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.3947C>T
  hgvsp: ENSP00000366310.1:p.Ala1316Val
  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.3947C>T
  hgvsp: ENSP00000379587.4:p.Ala1316Val
  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.3917C>T
  hgvsp: ENSP00000350791.3:p.Ala1306Val
  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.3955+376C>T
  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.3908C>T
  hgvsp: ENSP00000379581.1:p.Ala1303Val
  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.3917C>T
  hgvsp: ENSP00000354066.2:p.Ala1306Val
  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.4412C>T
  hgvsp: ENSP00000389542.3:p.Ala1471Val
  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.4343C>T
  hgvsp: ENSP00000350140.2:p.Ala1448Val
  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.3908C>T
  hgvsp: ENSP00000386127.2:p.Ala1303Val
  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.4331C>T
  hgvsp: ENSP00000366314.2:p.Ala1444Val
  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.3878C>T
  hgvsp: ENSP00000379576.5:p.Ala1293Val
  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.3908C>T
  hgvsp: ENSP00000366309.1:p.Ala1303Val
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1444Val
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

9-73151674-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151674
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151674
    reference: chr 9
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.4400C>T
  hgvsp: ENSP00000389542.3:p.Pro1467Leu
  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.3935C>T
  hgvsp: ENSP00000379587.4:p.Pro1312Leu
  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.3905C>T
  hgvsp: ENSP00000354066.2:p.Pro1302Leu
  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.3905C>T
  hgvsp: ENSP00000350791.3:p.Pro1302Leu
  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.4331C>T
  hgvsp: ENSP00000350140.2:p.Pro1444Leu
  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.4319C>T
  hgvsp: ENSP00000366314.2:p.Pro1440Leu
  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.3866C>T
  hgvsp: ENSP00000379576.5:p.Pro1289Leu
  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.3896C>T
  hgvsp: ENSP00000379581.1:p.Pro1299Leu
  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.3896C>T
  hgvsp: ENSP00000386127.2:p.Pro1299Leu
  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.3955+364C>T
  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.3935C>T
  hgvsp: ENSP00000366310.1:p.Pro1312Leu
  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.3896C>T
  hgvsp: ENSP00000366309.1:p.Pro1299Leu
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro1440Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

9-73151675-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151675
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151675
    reference: chr 9
allele count: 8
allele frequency: 6.589351607801793e-5
allele num: 121408
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.3904C>A
  hgvsp: ENSP00000354066.2:p.Pro1302Thr
  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.3955+363C>A
  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.3895C>A
  hgvsp: ENSP00000386127.2:p.Pro1299Thr
  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.3934C>A
  hgvsp: ENSP00000379587.4:p.Pro1312Thr
  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.3895C>A
  hgvsp: ENSP00000379581.1:p.Pro1299Thr
  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.3865C>A
  hgvsp: ENSP00000379576.5:p.Pro1289Thr
  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.3904C>A
  hgvsp: ENSP00000350791.3:p.Pro1302Thr
  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.3934C>A
  hgvsp: ENSP00000366310.1:p.Pro1312Thr
  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.4318C>A
  hgvsp: ENSP00000366314.2:p.Pro1440Thr
  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.3895C>A
  hgvsp: ENSP00000366309.1:p.Pro1299Thr
  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.4399C>A
  hgvsp: ENSP00000389542.3:p.Pro1467Thr
  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.4330C>A
  hgvsp: ENSP00000350140.2:p.Pro1444Thr
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6838
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1440Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

9-73151677-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151677
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151677
    reference: chr 9
allele count: 4
allele frequency: 3.294730079238259e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.3902C>T
  hgvsp: ENSP00000354066.2:p.Ala1301Val
  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.3902C>T
  hgvsp: ENSP00000350791.3:p.Ala1301Val
  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.3863C>T
  hgvsp: ENSP00000379576.5:p.Ala1288Val
  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.3955+361C>T
  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.4316C>T
  hgvsp: ENSP00000366314.2:p.Ala1439Val
  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.4397C>T
  hgvsp: ENSP00000389542.3:p.Ala1466Val
  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.3893C>T
  hgvsp: ENSP00000366309.1:p.Ala1298Val
  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.3893C>T
  hgvsp: ENSP00000379581.1:p.Ala1298Val
  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.4328C>T
  hgvsp: ENSP00000350140.2:p.Ala1443Val
  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.3932C>T
  hgvsp: ENSP00000379587.4:p.Ala1311Val
  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.3932C>T
  hgvsp: ENSP00000366310.1:p.Ala1311Val
  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.3893C>T
  hgvsp: ENSP00000386127.2:p.Ala1298Val
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6838
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala1439Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

9-73151688-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151688
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151688
    reference: chr 9
allele count: 12
allele frequency: 9.884027411702688e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.3891A>G
  hgvsp: ENST00000360823.2:c.3891A>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.3882A>G
  hgvsp: ENST00000408909.2:c.3882A>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.3891A>G
  hgvsp: ENST00000358082.3:c.3891A>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.4305A>G
  hgvsp: ENST00000377110.3:c.4305A>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.3852A>G
  hgvsp: ENST00000396280.5:c.3852A>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.3882A>G
  hgvsp: ENST00000377105.1:c.3882A>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.4317A>G
  hgvsp: ENST00000357533.2:c.4317A>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.3921A>G
  hgvsp: ENST00000377106.1:c.3921A>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.3921A>G
  hgvsp: ENST00000396292.4:c.3921A>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.3882A>G
  hgvsp: ENST00000396285.1:c.3882A>G(p.%3D)
  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.3955+350A>G
  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.4386A>G
  hgvsp: ENST00000423814.3:c.4386A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1435Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

9-73151691-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151691
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151691
    reference: chr 9
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
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.3849A>G
  hgvsp: ENST00000396280.5:c.3849A>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.3888A>G
  hgvsp: ENST00000360823.2:c.3888A>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.4302A>G
  hgvsp: ENST00000377110.3:c.4302A>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.3879A>G
  hgvsp: ENST00000377105.1:c.3879A>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.4314A>G
  hgvsp: ENST00000357533.2:c.4314A>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.3879A>G
  hgvsp: ENST00000408909.2:c.3879A>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.3918A>G
  hgvsp: ENST00000377106.1:c.3918A>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.4383A>G
  hgvsp: ENST00000423814.3:c.4383A>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.3879A>G
  hgvsp: ENST00000396285.1:c.3879A>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.3918A>G
  hgvsp: ENST00000396292.4:c.3918A>G(p.%3D)
  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.3955+347A>G
  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.3888A>G
  hgvsp: ENST00000358082.3:c.3888A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1434Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD

9-73151692-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151692
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151692
    reference: chr 9
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000366315
  ensembl transcript: ENST00000377111
  gene symbol: TRPM3
  hgvsc: ENST00000377111.2:c.3955+346C>T
  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.4301C>T
  hgvsp: ENSP00000366314.2:p.Pro1434Leu
  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.3887C>T
  hgvsp: ENSP00000350791.3:p.Pro1296Leu
  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.3878C>T
  hgvsp: ENSP00000379581.1:p.Pro1293Leu
  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.3878C>T
  hgvsp: ENSP00000386127.2:p.Pro1293Leu
  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.3917C>T
  hgvsp: ENSP00000366310.1:p.Pro1306Leu
  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.3848C>T
  hgvsp: ENSP00000379576.5:p.Pro1283Leu
  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.4313C>T
  hgvsp: ENSP00000350140.2:p.Pro1438Leu
  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.4382C>T
  hgvsp: ENSP00000389542.3:p.Pro1461Leu
  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.3917C>T
  hgvsp: ENSP00000379587.4:p.Pro1306Leu
  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.3887C>T
  hgvsp: ENSP00000354066.2:p.Pro1296Leu
  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.3878C>T
  hgvsp: ENSP00000366309.1:p.Pro1293Leu
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6839
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1434Leu
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: G
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

9-73151704-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151704
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151704
    reference: chr 9
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.3875G>C
  hgvsp: ENSP00000354066.2:p.Ser1292Thr
  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.3866G>C
  hgvsp: ENSP00000366309.1:p.Ser1289Thr
  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.3905G>C
  hgvsp: ENSP00000379587.4:p.Ser1302Thr
  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.3866G>C
  hgvsp: ENSP00000379581.1:p.Ser1289Thr
  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.3866G>C
  hgvsp: ENSP00000386127.2:p.Ser1289Thr
  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.3836G>C
  hgvsp: ENSP00000379576.5:p.Ser1279Thr
  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.4370G>C
  hgvsp: ENSP00000389542.3:p.Ser1457Thr
  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.4289G>C
  hgvsp: ENSP00000366314.2:p.Ser1430Thr
  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.3905G>C
  hgvsp: ENSP00000366310.1:p.Ser1302Thr
  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.3875G>C
  hgvsp: ENSP00000350791.3:p.Ser1292Thr
  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.4301G>C
  hgvsp: ENSP00000350140.2:p.Ser1434Thr
  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.3955+334G>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6839
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser1430Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

9-73151708-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151708
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151708
    reference: chr 9
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000389542
  ensembl transcript: ENST00000423814
  gene symbol: TRPM3
  hgvsc: ENST00000423814.3:c.4366C>T
  hgvsp: ENSP00000389542.3:p.Pro1456Ser
  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.3955+330C>T
  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.4285C>T
  hgvsp: ENSP00000366314.2:p.Pro1429Ser
  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.3901C>T
  hgvsp: ENSP00000379587.4:p.Pro1301Ser
  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.3862C>T
  hgvsp: ENSP00000386127.2:p.Pro1288Ser
  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.3871C>T
  hgvsp: ENSP00000354066.2:p.Pro1291Ser
  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.3862C>T
  hgvsp: ENSP00000366309.1:p.Pro1288Ser
  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.3871C>T
  hgvsp: ENSP00000350791.3:p.Pro1291Ser
  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.3862C>T
  hgvsp: ENSP00000379581.1:p.Pro1288Ser
  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.3832C>T
  hgvsp: ENSP00000379576.5:p.Pro1278Ser
  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.4297C>T
  hgvsp: ENSP00000350140.2:p.Pro1433Ser
  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.3901C>T
  hgvsp: ENSP00000366310.1:p.Pro1301Ser
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3939
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1429Ser
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

9-73151711-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151711
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151711
    reference: chr 9
allele count: 5
allele frequency: 4.11834475487612e-5
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000379587
  ensembl transcript: ENST00000396292
  gene symbol: TRPM3
  hgvsc: ENST00000396292.4:c.3898G>A
  hgvsp: ENSP00000379587.4:p.Glu1300Lys
  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.3859G>A
  hgvsp: ENSP00000379581.1:p.Glu1287Lys
  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.4282G>A
  hgvsp: ENSP00000366314.2:p.Glu1428Lys
  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.3898G>A
  hgvsp: ENSP00000366310.1:p.Glu1300Lys
  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.3955+327G>A
  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.3868G>A
  hgvsp: ENSP00000354066.2:p.Glu1290Lys
  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.3859G>A
  hgvsp: ENSP00000386127.2:p.Glu1287Lys
  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.4294G>A
  hgvsp: ENSP00000350140.2:p.Glu1432Lys
  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.3829G>A
  hgvsp: ENSP00000379576.5:p.Glu1277Lys
  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.3868G>A
  hgvsp: ENSP00000350791.3:p.Glu1290Lys
  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.4363G>A
  hgvsp: ENSP00000389542.3:p.Glu1455Lys
  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.3859G>A
  hgvsp: ENSP00000366309.1:p.Glu1287Lys
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6839
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu1428Lys
num of homozygotes: 1
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

9-73151712-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151712
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151712
    reference: chr 9
allele count: 6
allele frequency: 4.942257952916756e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000354066
  ensembl transcript: ENST00000360823
  gene symbol: TRPM3
  hgvsc: ENST00000360823.2:c.3867C>T
  hgvsp: ENST00000360823.2:c.3867C>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.3858C>T
  hgvsp: ENST00000408909.2:c.3858C>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.3897C>T
  hgvsp: ENST00000377106.1:c.3897C>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.3867C>T
  hgvsp: ENST00000358082.3:c.3867C>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.3858C>T
  hgvsp: ENST00000396285.1:c.3858C>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.4293C>T
  hgvsp: ENST00000357533.2:c.4293C>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.3828C>T
  hgvsp: ENST00000396280.5:c.3828C>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.4362C>T
  hgvsp: ENST00000423814.3:c.4362C>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.3897C>T
  hgvsp: ENST00000396292.4:c.3897C>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.4281C>T
  hgvsp: ENST00000377110.3:c.4281C>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.3858C>T
  hgvsp: ENST00000377105.1:c.3858C>T(p.%3D)
  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.3955+326C>T
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3962
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1427Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

9-73151712-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151712
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151712
    reference: chr 9
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000350140
  ensembl transcript: ENST00000357533
  gene symbol: TRPM3
  hgvsc: ENST00000357533.2:c.4293C>G
  hgvsp: ENST00000357533.2:c.4293C>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.3858C>G
  hgvsp: ENST00000408909.2:c.3858C>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.3897C>G
  hgvsp: ENST00000377106.1:c.3897C>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.3897C>G
  hgvsp: ENST00000396292.4:c.3897C>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.3828C>G
  hgvsp: ENST00000396280.5:c.3828C>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.3858C>G
  hgvsp: ENST00000396285.1:c.3858C>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.3867C>G
  hgvsp: ENST00000358082.3:c.3867C>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.3867C>G
  hgvsp: ENST00000360823.2:c.3867C>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.3858C>G
  hgvsp: ENST00000377105.1:c.3858C>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.4362C>G
  hgvsp: ENST00000423814.3:c.4362C>G(p.%3D)
  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.3955+326C>G
  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.4281C>G
  hgvsp: ENST00000377110.3:c.4281C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6847
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1427Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

9-73151715-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151715
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151715
    reference: chr 9
allele count: 103909
allele frequency: 8.558661702688456e-1
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.3855G>A
  hgvsp: ENST00000408909.2:c.3855G>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.3825G>A
  hgvsp: ENST00000396280.5:c.3825G>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.3894G>A
  hgvsp: ENST00000377106.1:c.3894G>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.3855G>A
  hgvsp: ENST00000377105.1:c.3855G>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.4359G>A
  hgvsp: ENST00000423814.3:c.4359G>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.4278G>A
  hgvsp: ENST00000377110.3:c.4278G>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.3864G>A
  hgvsp: ENST00000360823.2:c.3864G>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.3864G>A
  hgvsp: ENST00000358082.3:c.3864G>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.4290G>A
  hgvsp: ENST00000357533.2:c.4290G>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.3894G>A
  hgvsp: ENST00000396292.4:c.3894G>A(p.%3D)
  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.3955+323G>A
  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.3855G>A
  hgvsp: ENST00000396285.1:c.3855G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 6.75e1
  variant carriers: 2761
genotype depth: GenotypeDepth
  all individuals: 28158
  bin: 9.75e1
  variant carriers: 28158
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 5.25e1
  variant carriers: 1723
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.75e1
  variant carriers: 1318
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 8.75e1
  variant carriers: 3959
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 2.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 6.25e1
  variant carriers: 2431
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 8.25e1
  variant carriers: 3813
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 9.25e1
  variant carriers: 3871
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.25e1
  variant carriers: 318
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 7.25e1
  variant carriers: 3166
genotype quality: GenotypeQuality
hgvs: p.Leu1426Leu
num of homozygotes: 44800
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

9-73151720-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73151720
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 73151720
    reference: chr 9
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000083067
  ensembl protein: ENSP00000386127
  ensembl transcript: ENST00000408909
  gene symbol: TRPM3
  hgvsc: ENST00000408909.2:c.3850G>C
  hgvsp: ENSP00000386127.2:p.Gly1284Arg
  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.4354G>C
  hgvsp: ENSP00000389542.3:p.Gly1452Arg
  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.3859G>C
  hgvsp: ENSP00000354066.2:p.Gly1287Arg
  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.3859G>C
  hgvsp: ENSP00000350791.3:p.Gly1287Arg
  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.3889G>C
  hgvsp: ENSP00000379587.4:p.Gly1297Arg
  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.3850G>C
  hgvsp: ENSP00000379581.1:p.Gly1284Arg
  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.3850G>C
  hgvsp: ENSP00000366309.1:p.Gly1284Arg
  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.4273G>C
  hgvsp: ENSP00000366314.2:p.Gly1425Arg
  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.3820G>C
  hgvsp: ENSP00000379576.5:p.Gly1274Arg
  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.3889G>C
  hgvsp: ENSP00000366310.1:p.Gly1297Arg
  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.4285G>C
  hgvsp: ENSP00000350140.2:p.Gly1429Arg
  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.3955+318G>C
  variant of: http://identifiers.org/hgnc/17992
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15439
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1425Arg
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 3879
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4439
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3405
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5227
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1270
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4069
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1900
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48499
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 1174
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1423
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
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: 16508
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.24e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.076e0

DP
type: SiteQuality
SIO_000300: 3.925365e6

MQRankSum
type: SiteQuality
SIO_000300: -2.07e-1

FS
type: SiteQuality
SIO_000300: 5.05e0

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

QD
type: SiteQuality
SIO_000300: 1.23e1

GenotypeDepth
all individuals: 4988
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3404
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2779
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48498
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1271
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4072
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
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: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.26e-1

MQ
type: SiteQuality
SIO_000300: 6.033e1

FS
type: SiteQuality
SIO_000300: 6.357e0

QD
type: SiteQuality
SIO_000300: 1.211e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -8.0e-2

DP
type: SiteQuality
SIO_000300: 3.925431e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.11e-1

GenotypeDepth
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4988
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2158
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4438
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1895
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1286
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48497
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1269
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4070
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
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

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

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

QD
type: SiteQuality
SIO_000300: 1.303e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.996e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-2

DP
type: SiteQuality
SIO_000300: 3.925253e6

MQRankSum
type: SiteQuality
SIO_000300: 6.14e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.928e0

GenotypeDepth
all individuals: 2742
bin: 8.75e1
variant carriers: 35

GenotypeDepth
all individuals: 4427
bin: 7.25e1
variant carriers: 20

GenotypeDepth
all individuals: 3407
bin: 8.25e1
variant carriers: 45

GenotypeDepth
all individuals: 4982
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1284
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1888
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4070
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48515
bin: 9.75e1
variant carriers: 416

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.090380421613763e-3
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 120
allele frequency: 1.814333232537043e-2
allele num: 6614
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 280
allele frequency: 4.196768488264037e-3
allele num: 66718
num of homozygotes: 5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.23e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.863e0

MQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

QD
type: SiteQuality
SIO_000300: 1.358e1

DP
type: SiteQuality
SIO_000300: 3.928467e6

FS
type: SiteQuality
SIO_000300: 1.094e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.47e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

GenotypeDepth
all individuals: 3975
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5248
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3390
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1555
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48473
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1272
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4040
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

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

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

African
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

South Asian
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Other
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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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InbreedingCoeff
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QD
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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Other
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South Asian
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Latino
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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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DP
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QD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 66670
num of homozygotes: 0

Other
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East Asian
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Latino
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South Asian
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European (Finnish)
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African
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MQ
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QD
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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South Asian
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Latino
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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FS
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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 frequency: 1.92789666473877e-4
allele num: 10374
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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QD
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FS
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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SIO_000300: -4.02e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 16506
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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DP
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FS
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VQSLOD
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SIO_000300: 6.09e-1

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 66662
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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South Asian
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MQ
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SIO_000300: 5.94e1

VQSLOD
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MQRankSum
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QD
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DP
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
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SIO_000300: 5.12e-1

ReadPosRankSum
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SIO_000300: 5.629999999999999e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

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

Other
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MQRankSum
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SIO_000300: 8.47e-1

ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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QD
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VQSLOD
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FS
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SIO_000300: 1.766e0

InbreedingCoeff
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SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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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East Asian
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African
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Other
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Latino
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South Asian
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allele num: 16506
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.450337512054001e-3
allele num: 10370
num of homozygotes: 0

East Asian
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European (Non-Finnish)
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Latino
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allele num: 11566
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European (Finnish)
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South Asian
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Other
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FS
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QD
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DP
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele frequency: 1.213297743266198e-4
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East Asian
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Other
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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FS
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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Latino
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DP
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QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6
allele frequency: 9.026356962330004e-5
allele num: 66472
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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South Asian
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African
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allele frequency: 5.846813486649776e-4
allele num: 10262
num of homozygotes: 0

Latino
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InbreedingCoeff
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ClippingRankSum
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DP
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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Other
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African
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allele num: 10368
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South Asian
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allele count: 0
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num of homozygotes: 0

Latino
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele count: 0
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num of homozygotes: 0

European (Finnish)
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East Asian
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South Asian
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African
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allele frequency: 1.928640308582449e-4
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Latino
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European (Non-Finnish)
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DP
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MQRankSum
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FS
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

East Asian
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Other
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African
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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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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variant carriers: 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 frequency: 0.0e0
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Latino
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allele frequency: 1.728608470181504e-4
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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MQRankSum
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QD
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ClippingRankSum
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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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ReadPosRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66640
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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Other
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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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DP
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

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

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

GenotypeQuality
all individuals: 1309
bin: 9.25e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

FS
type: SiteQuality
SIO_000300: 3.488e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

MQRankSum
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SIO_000300: 3.33e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

DP
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SIO_000300: 3.918833e6

ClippingRankSum
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SIO_000300: -2.136e0

VQSLOD
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SIO_000300: 2.26e-1

BaseQRankSum
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SIO_000300: -2.417e0

QD
type: SiteQuality
SIO_000300: 1.361e1

GenotypeDepth
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variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.94925928147304e-4
allele num: 66692
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
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allele count: 39
allele frequency: 2.363922899745424e-3
allele num: 16498
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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SIO_000300: 3.920094e6

BaseQRankSum
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SIO_000300: -4.16e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 998
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

Latino
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allele count: 6
allele frequency: 5.184033177812338e-4
allele num: 11574
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.475e1

DP
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SIO_000300: 3.920094e6

MQ
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SIO_000300: 5.96e1

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: 3.81e0

BaseQRankSum
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SIO_000300: -4.16e-1

ReadPosRankSum
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SIO_000300: 4.76e-1

ClippingRankSum
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SIO_000300: -3.38e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 3664
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
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MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.919779e6

BaseQRankSum
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SIO_000300: -1.047e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.85e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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SIO_000300: 1.144e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

Latino
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allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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QD
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MQ
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VQSLOD
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MQRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

Other
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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66720
num of homozygotes: 0

Latino
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num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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MQ
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QD
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

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

African
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allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

Latino
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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FS
type: SiteQuality
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MQ
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

African
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European (Non-Finnish)
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allele num: 66738
num of homozygotes: 0

Other
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European (Finnish)
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Latino
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South Asian
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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QD
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FS
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DP
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

Other
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European (Finnish)
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South Asian
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allele num: 16512
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Latino
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African
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East Asian
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ClippingRankSum
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FS
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BaseQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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East Asian
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Latino
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VQSLOD
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FS
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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Other
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East Asian
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European (Finnish)
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European (Non-Finnish)
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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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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African
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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DP
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ReadPosRankSum
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FS
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BaseQRankSum
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VQSLOD
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SIO_000300: 1.71e0

GenotypeDepth
all individuals: 3928
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6831
bin: 9.75e1
variant carriers: 1

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4413
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3750
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1541
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1916
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48499
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1347
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495190146543199e-5
allele num: 66738
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.557e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.77e-1

FS
type: SiteQuality
SIO_000300: 5.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

QD
type: SiteQuality
SIO_000300: 1.268e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 3.923976e6

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeDepth
all individuals: 3962
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6831
bin: 9.75e1
variant carriers: 1

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48499
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1310
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3747
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 3.924019e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.342e0

MQRankSum
type: SiteQuality
SIO_000300: -1.168e0

FS
type: SiteQuality
SIO_000300: 2.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 9.56e0

GenotypeDepth
all individuals: 4596
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2729
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3962
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4977
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1311
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1914
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48501
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3743
bin: 6.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.346e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.621e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-1

DP
type: SiteQuality
SIO_000300: 3.924087e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

FS
type: SiteQuality
SIO_000300: 3.238e0

VQSLOD
type: SiteQuality
SIO_000300: 8.96e-1

GenotypeDepth
all individuals: 5212
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3928
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2156
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6832
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3741
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1916
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
all individuals: 1312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48501
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
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: 908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.917e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.78e-1

DP
type: SiteQuality
SIO_000300: 3.924111e6

QD
type: SiteQuality
SIO_000300: 1.225e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.174e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 5.916e1

GenotypeDepth
all individuals: 4596
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3391
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4412
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1348
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1327
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 48501
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

Latino
type: Population
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 3.924152e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

QD
type: SiteQuality
SIO_000300: 1.129e1

FS
type: SiteQuality
SIO_000300: 2.413e0

VQSLOD
type: SiteQuality
SIO_000300: 9.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.491983577571999e-5
allele num: 66738
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.21e-1

QD
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SIO_000300: 1.302e1

BaseQRankSum
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SIO_000300: -3.563e0

InbreedingCoeff
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SIO_000300: 1.51e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.37e-1

VQSLOD
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SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

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

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

European (Finnish)
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allele 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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

East Asian
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num of homozygotes: 0

ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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BaseQRankSum
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VQSLOD
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DP
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SIO_000300: 3.92435e6

QD
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GenotypeDepth
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variant carriers: 2

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: 6.25e1
variant carriers: 0

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

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

South Asian
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allele num: 16512
num of homozygotes: 0

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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FS
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QD
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MQRankSum
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MQ
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ReadPosRankSum
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SIO_000300: 6.64e-1

InbreedingCoeff
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SIO_000300: 1.51e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
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MQ
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SIO_000300: 5.95e1

ReadPosRankSum
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SIO_000300: 8.52e-1

DP
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SIO_000300: 3.924421e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

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

Latino
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num of homozygotes: 0

Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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QD
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

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

African
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East Asian
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South Asian
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FS
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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num of homozygotes: 0

European (Finnish)
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European (Non-Finnish)
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Other
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East Asian
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African
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Latino
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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ReadPosRankSum
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DP
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FS
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 16512
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Other
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European (Non-Finnish)
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East Asian
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African
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Latino
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European (Finnish)
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QD
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FS
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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East Asian
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ReadPosRankSum
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FS
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DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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MQ
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QD
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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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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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East Asian
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DP
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VQSLOD
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FS
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MQ
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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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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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African
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QD
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MQ
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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VQSLOD
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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FS
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MQRankSum
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DP
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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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Latino
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African
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East Asian
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European (Finnish)
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MQ
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VQSLOD
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FS
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QD
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InbreedingCoeff
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DP
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African
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South Asian
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BaseQRankSum
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MQ
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DP
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MQ
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all individuals: 111
bin: 7.75e1
variant carriers: 27

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

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 92
bin: 7.25e1
variant carriers: 18

GenotypeQuality
all individuals: 253
bin: 6.75e1
variant carriers: 19

GenotypeQuality
all individuals: 103
bin: 8.25e1
variant carriers: 62

GenotypeQuality
all individuals: 58880
bin: 9.75e1
variant carriers: 58835

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 8

European (Finnish)
type: Population
allele count: 5779
allele frequency: 8.737526459026308e-1
allele num: 6614
num of homozygotes: 2519

East Asian
type: Population
allele count: 8455
allele frequency: 9.770048532470534e-1
allele num: 8654
num of homozygotes: 4130

African
type: Population
allele count: 8930
allele frequency: 8.581587545646743e-1
allele num: 10406
num of homozygotes: 3843

South Asian
type: Population
allele count: 11468
allele frequency: 6.945251937984496e-1
allele num: 16512
num of homozygotes: 4009

European (Non-Finnish)
type: Population
allele count: 57989
allele frequency: 8.689313114361065e-1
allele num: 66736
num of homozygotes: 25196

Other
type: Population
allele count: 765
allele frequency: 8.425110132158591e-1
allele num: 908
num of homozygotes: 325

Latino
type: Population
allele count: 10523
allele frequency: 9.088789082743134e-1
allele num: 11578
num of homozygotes: 4778

DP
type: SiteQuality
SIO_000300: 5.777861e6

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.72e-2

QD
type: SiteQuality
SIO_000300: 2.82e1

GenotypeDepth
all individuals: 3714
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3026
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3709
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9252
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 581
bin: 9.25e1
variant carriers: 0