1-155032426-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032426
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032424
    reference: chr 1
allele count: 2
allele frequency: 1.649974425396406e-5
allele num: 121214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1163_1164delCT
  hgvsp: ENSP00000357395.2:p.Pro388ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.128_129delCT
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2081_2082delCT
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2045_2046delCT
  hgvsp: ENSP00000357397.3:p.Pro682ArgfsTer134
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2045_2046delCT
  hgvsp: ENSP00000271836.6:p.Pro682ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2045_2046delCT
  hgvsp: ENSP00000403843.2:p.Pro682ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2045_2046delCT
  hgvsp: ENSP00000349436.2:p.Pro682ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1163_1164delCT
  hgvsp: ENSP00000357398.1:p.Pro388ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2175_2176delCT
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2045_2046delCT
  hgvsp: ENSP00000434227.1:p.Pro682ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2045_2046delCT
  hgvsp: ENSP00000353892.4:p.Pro682ArgfsTer110
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2075_2076delCT
  hgvsp: ENSP00000432927.1:p.Pro692ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2045_2046delCT
  hgvsp: ENSP00000348227.2:p.Pro682ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2045_2046delCT
  hgvsp: ENSP00000432347.1:p.Pro682ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.85_86delCT
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.324_325delCT
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.331_332delCT
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2045_2046delCT
  hgvsp: ENSP00000352226.4:p.Pro682ArgfsTer62
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3691_3692delCT
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro682ArgfsTer62
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: CCT
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-155032426-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032426
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032426
    reference: chr 1
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.84C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.323C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2044C>A
  hgvsp: ENSP00000271836.6:p.Pro682Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1162C>A
  hgvsp: ENSP00000357395.2:p.Pro388Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3690C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1162C>A
  hgvsp: ENSP00000357398.1:p.Pro388Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2044C>A
  hgvsp: ENSP00000352226.4:p.Pro682Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2044C>A
  hgvsp: ENSP00000357397.3:p.Pro682Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2044C>A
  hgvsp: ENSP00000432347.1:p.Pro682Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.127C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2044C>A
  hgvsp: ENSP00000349436.2:p.Pro682Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2044C>A
  hgvsp: ENSP00000403843.2:p.Pro682Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2044C>A
  hgvsp: ENSP00000353892.4:p.Pro682Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2044C>A
  hgvsp: ENSP00000348227.2:p.Pro682Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2044C>A
  hgvsp: ENSP00000434227.1:p.Pro682Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2174C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2080C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.330C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2074C>A
  hgvsp: ENSP00000432927.1:p.Pro692Thr
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro682Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

1-155032434-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032434
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032434
    reference: chr 1
allele count: 14
allele frequency: 1.155191761832464e-4
allele num: 121192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2052C>T
  hgvsp: ENST00000449910.2:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2182C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2082C>T
  hgvsp: ENST00000531455.1:c.2082C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1170C>T
  hgvsp: ENST00000368410.2:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.331C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1170C>T
  hgvsp: ENST00000368413.1:c.1170C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2052C>T
  hgvsp: ENST00000529473.1:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2052C>T
  hgvsp: ENST00000355956.2:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2052C>T
  hgvsp: ENST00000360674.4:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.92C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2052C>T
  hgvsp: ENST00000356955.2:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2052C>T
  hgvsp: ENST00000359280.4:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.135C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2052C>T
  hgvsp: ENST00000271836.6:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2052C>T
  hgvsp: ENST00000526491.1:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2052C>T
  hgvsp: ENST00000368412.3:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3698C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2088C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.338C>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys684Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-155032436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032436
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032436
    reference: chr 1
allele count: 2
allele frequency: 1.650437365901964e-5
allele num: 121180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2054C>T
  hgvsp: ENSP00000353892.4:p.Thr685Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1172C>T
  hgvsp: ENSP00000357395.2:p.Thr391Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2054C>T
  hgvsp: ENSP00000432347.1:p.Thr685Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2084C>T
  hgvsp: ENSP00000432927.1:p.Thr695Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2184C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2054C>T
  hgvsp: ENSP00000357397.3:p.Thr685Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2054C>T
  hgvsp: ENSP00000348227.2:p.Thr685Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2090C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2054C>T
  hgvsp: ENSP00000271836.6:p.Thr685Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.137C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2054C>T
  hgvsp: ENSP00000403843.2:p.Thr685Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.94C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.340C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2054C>T
  hgvsp: ENSP00000352226.4:p.Thr685Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1172C>T
  hgvsp: ENSP00000357398.1:p.Thr391Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2054C>T
  hgvsp: ENSP00000434227.1:p.Thr685Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3700C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.333C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2054C>T
  hgvsp: ENSP00000349436.2:p.Thr685Ile
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr685Ile
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-155032441-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032441
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032441
    reference: chr 1
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1177C>A
  hgvsp: ENSP00000357398.1:p.Gln393Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2059C>A
  hgvsp: ENSP00000432347.1:p.Gln687Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2059C>A
  hgvsp: ENSP00000357397.3:p.Gln687Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2059C>A
  hgvsp: ENSP00000434227.1:p.Gln687Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2059C>A
  hgvsp: ENSP00000353892.4:p.Gln687Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2059C>A
  hgvsp: ENSP00000403843.2:p.Gln687Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3705C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2059C>A
  hgvsp: ENSP00000348227.2:p.Gln687Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2059C>A
  hgvsp: ENSP00000271836.6:p.Gln687Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2059C>A
  hgvsp: ENSP00000349436.2:p.Gln687Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2089C>A
  hgvsp: ENSP00000432927.1:p.Gln697Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1177C>A
  hgvsp: ENSP00000357395.2:p.Gln393Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.142C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2059C>A
  hgvsp: ENSP00000352226.4:p.Gln687Lys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.345C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.99C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2095C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.338C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2189C>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln687Lys
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

1-155032450-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032450
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032450
    reference: chr 1
allele count: 1
allele frequency: 8.258320257659592e-6
allele num: 121090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068G>C
  hgvsp: ENSP00000271836.6:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068G>C
  hgvsp: ENSP00000353892.4:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068G>C
  hgvsp: ENSP00000434227.1:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068G>C
  hgvsp: ENSP00000432347.1:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068G>C
  hgvsp: ENSP00000348227.2:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068G>C
  hgvsp: ENSP00000352226.4:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186G>C
  hgvsp: ENSP00000357395.2:p.Ala396Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098G>C
  hgvsp: ENSP00000432927.1:p.Ala700Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186G>C
  hgvsp: ENSP00000357398.1:p.Ala396Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068G>C
  hgvsp: ENSP00000357397.3:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068G>C
  hgvsp: ENSP00000349436.2:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068G>C
  hgvsp: ENSP00000403843.2:p.Ala690Pro
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala690Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS

1-155032455-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032455
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032455
    reference: chr 1
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+5C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+5C>G
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2068+5C>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

1-155032458-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032458
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032458
    reference: chr 1
allele count: 2
allele frequency: 1.65264671371201e-5
allele num: 121018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+8G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2068+8G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

1-155032463-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032463
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032463
    reference: chr 1
allele count: 1
allele frequency: 8.265145879824779e-6
allele num: 120990
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+13T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+13T>G
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

1-155032470-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032470
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032468
    reference: chr 1
allele count: 6
allele frequency: 4.960973673766371e-5
allele num: 120944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+21_2068+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+21_1186+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+21_2068+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+21_2068+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+21_354+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+21_3714+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+21_2068+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+21_151+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+21_2068+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+21_2198+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+21_347+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+21_108+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+21_2068+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+21_2068+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+21_2098+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+21_1186+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+21_2068+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+21_2104+22delAG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+21_2068+22delAG
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: CAG
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

1-155032475-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032475
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032475
    reference: chr 1
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+25G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+25G>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

1-155032478-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032478
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032478
    reference: chr 1
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+28G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+28G>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

1-155032482-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032482
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032482
    reference: chr 1
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+32G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+32G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-155032483-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032483
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032483
    reference: chr 1
allele count: 8
allele frequency: 6.620981891614527e-5
allele num: 120828
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+33G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+33G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

1-155032485-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032485
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032485
    reference: chr 1
allele count: 1
allele frequency: 8.279927799029592e-6
allele num: 120774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+35G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+35G>C
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-155032488-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032488
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032487
    reference: chr 1
allele count: 1
allele frequency: 8.286651861182008e-6
allele num: 120676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+41delA
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+41delA
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4626
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: CA
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

1-155032492-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032492
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032492
    reference: chr 1
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+42G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+42G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

1-155032494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032494
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032494
    reference: chr 1
allele count: 19
allele frequency: 1.574672633847174e-4
allele num: 120660
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+44G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+44G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4907
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

1-155032494-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032494
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032494
    reference: chr 1
allele count: 1
allele frequency: 8.28775070445881e-6
allele num: 120660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+44G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+44G>C
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

1-155032498-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032498
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032498
    reference: chr 1
allele count: 1
allele frequency: 8.29242404139578e-6
allele num: 120592
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.108+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2068+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2068+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2068+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2068+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.354+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2068+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2068+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2068+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.347+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.151+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2098+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1186+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1186+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2104+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2068+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2198+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2068+48C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3714+48C>G
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4924
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

1-155032638-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032638
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032638
    reference: chr 1
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-43G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-43G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

1-155032649-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032649
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032649
    reference: chr 1
allele count: 4
allele frequency: 3.316144650229643e-5
allele num: 120622
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-32C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-32C>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-155032650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032650
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032650
    reference: chr 1
allele count: 3
allele frequency: 2.486366424107809e-5
allele num: 120658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-31G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-31G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

1-155032651-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032651
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032651
    reference: chr 1
allele count: 5
allele frequency: 4.142982616044943e-5
allele num: 120686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-30T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-30T>C
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

1-155032654-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032654
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032653
    reference: chr 1
allele count: 4
allele frequency: 3.312025966283576e-5
allele num: 120772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-24delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-24delC
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6824
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: TC
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

1-155032662-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032662
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032662
    reference: chr 1
allele count: 2
allele frequency: 1.654095540558423e-5
allele num: 120912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-19A>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-19A>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6820
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

1-155032668-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032668
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032668
    reference: chr 1
allele count: 1
allele frequency: 8.265282507356101e-6
allele num: 120988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-13C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-13C>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4176
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

1-155032670-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032670
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032669
    reference: chr 1
allele count: 427
allele frequency: 3.528050896471949e-3
allele num: 121030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-9delC
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-9delC
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: TC
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

1-155032672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032672
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032672
    reference: chr 1
allele count: 1
allele frequency: 8.322375538873816e-6
allele num: 120158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-9C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-9C>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

1-155032673-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032673
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032673
    reference: chr 1
allele count: 4
allele frequency: 3.30436506625252e-5
allele num: 121052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1187-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2069-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2069-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2105-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.109-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2199-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.152-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1187-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2069-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2069-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3715-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2069-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.348-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.355-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2069-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2069-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2069-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2069-8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2099-8G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2069-8G>A
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

1-155032712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032712
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032712
    reference: chr 1
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2100C>T
  hgvsp: ENST00000359280.4:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.140C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2100C>T
  hgvsp: ENST00000271836.6:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1218C>T
  hgvsp: ENST00000368413.1:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2100C>T
  hgvsp: ENST00000368412.3:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2130C>T
  hgvsp: ENST00000531455.1:c.2130C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2100C>T
  hgvsp: ENST00000360674.4:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2100C>T
  hgvsp: ENST00000449910.2:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2100C>T
  hgvsp: ENST00000355956.2:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2100C>T
  hgvsp: ENST00000356955.2:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1218C>T
  hgvsp: ENST00000368410.2:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.183C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2100C>T
  hgvsp: ENST00000526491.1:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.379C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2100C>T
  hgvsp: ENST00000529473.1:c.2100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2136C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3746C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2230C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.386C>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu700Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-155032722-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032722
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032722
    reference: chr 1
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3756G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2146G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2110G>C
  hgvsp: ENSP00000348227.2:p.Val704Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1228G>C
  hgvsp: ENSP00000357398.1:p.Val410Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.396G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2110G>C
  hgvsp: ENSP00000271836.6:p.Val704Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2110G>C
  hgvsp: ENSP00000352226.4:p.Val704Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2140G>C
  hgvsp: ENSP00000432927.1:p.Val714Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2110G>C
  hgvsp: ENSP00000357397.3:p.Val704Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2110G>C
  hgvsp: ENSP00000353892.4:p.Val704Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2110G>C
  hgvsp: ENSP00000434227.1:p.Val704Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2110G>C
  hgvsp: ENSP00000432347.1:p.Val704Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2110G>C
  hgvsp: ENSP00000349436.2:p.Val704Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2240G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.150G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1228G>C
  hgvsp: ENSP00000357395.2:p.Val410Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.193G>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2110G>C
  hgvsp: ENSP00000403843.2:p.Val704Leu
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.389G>C
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val704Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-155032732-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032732
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032732
    reference: chr 1
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2120T>C
  hgvsp: ENSP00000403843.2:p.Val707Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.203T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2120T>C
  hgvsp: ENSP00000432347.1:p.Val707Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2150T>C
  hgvsp: ENSP00000432927.1:p.Val717Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.399T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2120T>C
  hgvsp: ENSP00000434227.1:p.Val707Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2120T>C
  hgvsp: ENSP00000349436.2:p.Val707Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2120T>C
  hgvsp: ENSP00000353892.4:p.Val707Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1238T>C
  hgvsp: ENSP00000357398.1:p.Val413Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2250T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.160T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2120T>C
  hgvsp: ENSP00000357397.3:p.Val707Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2120T>C
  hgvsp: ENSP00000348227.2:p.Val707Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2156T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3766T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2120T>C
  hgvsp: ENSP00000271836.6:p.Val707Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.406T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2120T>C
  hgvsp: ENSP00000352226.4:p.Val707Ala
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1238T>C
  hgvsp: ENSP00000357395.2:p.Val413Ala
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val707Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

1-155032735-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032735
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032735
    reference: chr 1
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2123T>G
  hgvsp: ENSP00000403843.2:p.Leu708Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.206T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2253T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2123T>G
  hgvsp: ENSP00000349436.2:p.Leu708Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1241T>G
  hgvsp: ENSP00000357395.2:p.Leu414Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2123T>G
  hgvsp: ENSP00000348227.2:p.Leu708Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2123T>G
  hgvsp: ENSP00000352226.4:p.Leu708Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2123T>G
  hgvsp: ENSP00000271836.6:p.Leu708Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2153T>G
  hgvsp: ENSP00000432927.1:p.Leu718Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2123T>G
  hgvsp: ENSP00000357397.3:p.Leu708Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1241T>G
  hgvsp: ENSP00000357398.1:p.Leu414Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2123T>G
  hgvsp: ENSP00000432347.1:p.Leu708Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2123T>G
  hgvsp: ENSP00000434227.1:p.Leu708Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2123T>G
  hgvsp: ENSP00000353892.4:p.Leu708Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.402T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.409T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.163T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3769T>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2159T>G
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu708Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

1-155032736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032736
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032736
    reference: chr 1
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2124G>A
  hgvsp: ENST00000359280.4:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1242G>A
  hgvsp: ENST00000368410.2:c.1242G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2124G>A
  hgvsp: ENST00000526491.1:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.403G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3770G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2124G>A
  hgvsp: ENST00000368412.3:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.410G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2124G>A
  hgvsp: ENST00000449910.2:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.207G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2124G>A
  hgvsp: ENST00000271836.6:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2124G>A
  hgvsp: ENST00000360674.4:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2124G>A
  hgvsp: ENST00000355956.2:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2124G>A
  hgvsp: ENST00000356955.2:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2124G>A
  hgvsp: ENST00000529473.1:c.2124G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1242G>A
  hgvsp: ENST00000368413.1:c.1242G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2160G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2254G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2154G>A
  hgvsp: ENST00000531455.1:c.2154G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.164G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu708Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

1-155032742-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032742
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032742
    reference: chr 1
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2260G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2130G>A
  hgvsp: ENSP00000348227.2:p.Met710Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2160G>A
  hgvsp: ENSP00000432927.1:p.Met720Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2130G>A
  hgvsp: ENSP00000403843.2:p.Met710Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.1G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2130G>A
  hgvsp: ENSP00000434227.1:p.Met710Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2130G>A
  hgvsp: ENSP00000353892.4:p.Met710Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.170G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1248G>A
  hgvsp: ENSP00000357398.1:p.Met416Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.416G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2130G>A
  hgvsp: ENSP00000352226.4:p.Met710Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2166G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2130G>A
  hgvsp: ENSP00000432347.1:p.Met710Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1248G>A
  hgvsp: ENSP00000357395.2:p.Met416Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3776G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2130G>A
  hgvsp: ENSP00000357397.3:p.Met710Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.409G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.213G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2130G>A
  hgvsp: ENSP00000349436.2:p.Met710Ile
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2130G>A
  hgvsp: ENSP00000271836.6:p.Met710Ile
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met710Ile
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

1-155032749-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032749
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032749
    reference: chr 1
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2137G>A
  hgvsp: ENSP00000352226.4:p.Ala713Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.416G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1255G>A
  hgvsp: ENSP00000357395.2:p.Ala419Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2137G>A
  hgvsp: ENSP00000348227.2:p.Ala713Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2167G>A
  hgvsp: ENSP00000432927.1:p.Ala723Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.177G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2137G>A
  hgvsp: ENSP00000434227.1:p.Ala713Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2137G>A
  hgvsp: ENSP00000403843.2:p.Ala713Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2137G>A
  hgvsp: ENSP00000357397.3:p.Ala713Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.8G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.220G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2137G>A
  hgvsp: ENSP00000432347.1:p.Ala713Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3783G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2137G>A
  hgvsp: ENSP00000349436.2:p.Ala713Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1255G>A
  hgvsp: ENSP00000357398.1:p.Ala419Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2137G>A
  hgvsp: ENSP00000353892.4:p.Ala713Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.423G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2137G>A
  hgvsp: ENSP00000271836.6:p.Ala713Thr
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2173G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2267G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala713Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

1-155032752-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032752
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032752
    reference: chr 1
allele count: 1305
allele frequency: 1.076785979503936e-2
allele num: 121194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1258A>G
  hgvsp: ENSP00000357395.2:p.Ser420Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2176A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2140A>G
  hgvsp: ENSP00000352226.4:p.Ser714Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.426A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2270A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2140A>G
  hgvsp: ENSP00000353892.4:p.Ser714Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2140A>G
  hgvsp: ENSP00000434227.1:p.Ser714Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.419A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1258A>G
  hgvsp: ENSP00000357398.1:p.Ser420Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.11A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3786A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2140A>G
  hgvsp: ENSP00000357397.3:p.Ser714Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2170A>G
  hgvsp: ENSP00000432927.1:p.Ser724Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2140A>G
  hgvsp: ENSP00000403843.2:p.Ser714Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2140A>G
  hgvsp: ENSP00000348227.2:p.Ser714Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2140A>G
  hgvsp: ENSP00000432347.1:p.Ser714Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2140A>G
  hgvsp: ENSP00000271836.6:p.Ser714Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.223A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2140A>G
  hgvsp: ENSP00000349436.2:p.Ser714Gly
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.180A>G
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser714Gly
num of homozygotes: 82
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

1-155032761-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032761
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032761
    reference: chr 1
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2149T>C
  hgvsp: ENSP00000403843.2:p.Tyr717His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.20T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.189T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2149T>C
  hgvsp: ENSP00000352226.4:p.Tyr717His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2185T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2149T>C
  hgvsp: ENSP00000434227.1:p.Tyr717His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2149T>C
  hgvsp: ENSP00000348227.2:p.Tyr717His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2149T>C
  hgvsp: ENSP00000432347.1:p.Tyr717His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2149T>C
  hgvsp: ENSP00000271836.6:p.Tyr717His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2149T>C
  hgvsp: ENSP00000353892.4:p.Tyr717His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3795T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1267T>C
  hgvsp: ENSP00000357398.1:p.Tyr423His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.232T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2149T>C
  hgvsp: ENSP00000357397.3:p.Tyr717His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2279T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.428T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2179T>C
  hgvsp: ENSP00000432927.1:p.Tyr727His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.435T>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2149T>C
  hgvsp: ENSP00000349436.2:p.Tyr717His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1267T>C
  hgvsp: ENSP00000357395.2:p.Tyr423His
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Tyr717His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

1-155032762-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032762
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032762
    reference: chr 1
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2150A>G
  hgvsp: ENSP00000349436.2:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2150A>G
  hgvsp: ENSP00000403843.2:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1268A>G
  hgvsp: ENSP00000357398.1:p.Tyr423Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2150A>G
  hgvsp: ENSP00000271836.6:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.429A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2150A>G
  hgvsp: ENSP00000353892.4:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2150A>G
  hgvsp: ENSP00000434227.1:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2186A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.233A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2150A>G
  hgvsp: ENSP00000432347.1:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2180A>G
  hgvsp: ENSP00000432927.1:p.Tyr727Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1268A>G
  hgvsp: ENSP00000357395.2:p.Tyr423Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.190A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.21A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2150A>G
  hgvsp: ENSP00000348227.2:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2150A>G
  hgvsp: ENSP00000357397.3:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2280A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.436A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3796A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2150A>G
  hgvsp: ENSP00000352226.4:p.Tyr717Cys
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Tyr717Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-155032764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032764
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032764
    reference: chr 1
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2152C>T
  hgvsp: ENSP00000357397.3:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2152C>T
  hgvsp: ENSP00000271836.6:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.192C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1270C>T
  hgvsp: ENSP00000357395.2:p.Arg424Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1270C>T
  hgvsp: ENSP00000357398.1:p.Arg424Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2152C>T
  hgvsp: ENSP00000348227.2:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3798C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.235C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2152C>T
  hgvsp: ENSP00000353892.4:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2152C>T
  hgvsp: ENSP00000403843.2:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2152C>T
  hgvsp: ENSP00000432347.1:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2182C>T
  hgvsp: ENSP00000432927.1:p.Arg728Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2188C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2152C>T
  hgvsp: ENSP00000352226.4:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.431C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2282C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.23C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2152C>T
  hgvsp: ENSP00000349436.2:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.438C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2152C>T
  hgvsp: ENSP00000434227.1:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg718Cys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum

1-155032765-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032765
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032765
    reference: chr 1
allele count: 7
allele frequency: 5.776912157924273e-5
allele num: 121172
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3799G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2153G>A
  hgvsp: ENSP00000271836.6:p.Arg718His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.439G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1271G>A
  hgvsp: ENSP00000357395.2:p.Arg424His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2153G>A
  hgvsp: ENSP00000348227.2:p.Arg718His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2183G>A
  hgvsp: ENSP00000432927.1:p.Arg728His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2153G>A
  hgvsp: ENSP00000352226.4:p.Arg718His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2283G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2153G>A
  hgvsp: ENSP00000357397.3:p.Arg718His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1271G>A
  hgvsp: ENSP00000357398.1:p.Arg424His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2153G>A
  hgvsp: ENSP00000349436.2:p.Arg718His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2153G>A
  hgvsp: ENSP00000432347.1:p.Arg718His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.236G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.432G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2153G>A
  hgvsp: ENSP00000353892.4:p.Arg718His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2153G>A
  hgvsp: ENSP00000403843.2:p.Arg718His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.24G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2189G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2153G>A
  hgvsp: ENSP00000434227.1:p.Arg718His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.193G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg718His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

1-155032768-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032768
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032768
    reference: chr 1
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2156C>T
  hgvsp: ENSP00000348227.2:p.Ala719Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2156C>T
  hgvsp: ENSP00000432347.1:p.Ala719Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2192C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.239C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1274C>T
  hgvsp: ENSP00000357395.2:p.Ala425Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2156C>T
  hgvsp: ENSP00000353892.4:p.Ala719Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2186C>T
  hgvsp: ENSP00000432927.1:p.Ala729Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2156C>T
  hgvsp: ENSP00000357397.3:p.Ala719Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.27C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2156C>T
  hgvsp: ENSP00000349436.2:p.Ala719Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2156C>T
  hgvsp: ENSP00000434227.1:p.Ala719Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.442C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2156C>T
  hgvsp: ENSP00000403843.2:p.Ala719Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1274C>T
  hgvsp: ENSP00000357398.1:p.Ala425Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2156C>T
  hgvsp: ENSP00000271836.6:p.Ala719Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2156C>T
  hgvsp: ENSP00000352226.4:p.Ala719Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.435C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.196C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2286C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3802C>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala719Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

1-155032770-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032770
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032770
    reference: chr 1
allele count: 2
allele frequency: 1.650192247396822e-5
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1276C>T
  hgvsp: ENSP00000357395.2:p.Arg426Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2188C>T
  hgvsp: ENSP00000432927.1:p.Arg730Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.437C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1276C>T
  hgvsp: ENSP00000357398.1:p.Arg426Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2194C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2158C>T
  hgvsp: ENSP00000348227.2:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2158C>T
  hgvsp: ENSP00000357397.3:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2158C>T
  hgvsp: ENSP00000353892.4:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2158C>T
  hgvsp: ENSP00000403843.2:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.29C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2288C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2158C>T
  hgvsp: ENSP00000432347.1:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2158C>T
  hgvsp: ENSP00000349436.2:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2158C>T
  hgvsp: ENSP00000271836.6:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.241C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2158C>T
  hgvsp: ENSP00000352226.4:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.444C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3804C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.198C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2158C>T
  hgvsp: ENSP00000434227.1:p.Arg720Cys
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg720Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

1-155032771-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032771
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032771
    reference: chr 1
allele count: 37
allele frequency: 3.053057182935886e-4
allele num: 121190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2195G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.445G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2189G>A
  hgvsp: ENSP00000432927.1:p.Arg730His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2159G>A
  hgvsp: ENSP00000434227.1:p.Arg720His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1277G>A
  hgvsp: ENSP00000357395.2:p.Arg426His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2159G>A
  hgvsp: ENSP00000353892.4:p.Arg720His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.242G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2159G>A
  hgvsp: ENSP00000349436.2:p.Arg720His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2159G>A
  hgvsp: ENSP00000432347.1:p.Arg720His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.30G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2159G>A
  hgvsp: ENSP00000352226.4:p.Arg720His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.438G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.199G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2159G>A
  hgvsp: ENSP00000348227.2:p.Arg720His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2159G>A
  hgvsp: ENSP00000271836.6:p.Arg720His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1277G>A
  hgvsp: ENSP00000357398.1:p.Arg426His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3805G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2159G>A
  hgvsp: ENSP00000403843.2:p.Arg720His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2159G>A
  hgvsp: ENSP00000357397.3:p.Arg720His
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2289G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg720His
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

1-155032778-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032778
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032778
    reference: chr 1
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2166C>T
  hgvsp: ENST00000526491.1:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2296C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2166C>T
  hgvsp: ENST00000271836.6:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2166C>T
  hgvsp: ENST00000449910.2:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2166C>T
  hgvsp: ENST00000356955.2:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2166C>T
  hgvsp: ENST00000359280.4:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2166C>T
  hgvsp: ENST00000360674.4:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2166C>T
  hgvsp: ENST00000355956.2:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2196C>T
  hgvsp: ENST00000531455.1:c.2196C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.249C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3812C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1284C>T
  hgvsp: ENST00000368413.1:c.1284C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2166C>T
  hgvsp: ENST00000368412.3:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2166C>T
  hgvsp: ENST00000529473.1:c.2166C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1284C>T
  hgvsp: ENST00000368410.2:c.1284C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.452C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.445C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2202C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.37C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.206C>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His722His
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

1-155032782-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032782
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032782
    reference: chr 1
allele count: 4
allele frequency: 3.299894403379092e-5
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2206C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.210C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2170C>T
  hgvsp: ENSP00000353892.4:p.Arg724Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.253C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3816C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2170C>T
  hgvsp: ENSP00000434227.1:p.Arg724Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2170C>T
  hgvsp: ENSP00000357397.3:p.Arg724Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1288C>T
  hgvsp: ENSP00000357398.1:p.Arg430Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1288C>T
  hgvsp: ENSP00000357395.2:p.Arg430Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2300C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2200C>T
  hgvsp: ENSP00000432927.1:p.Arg734Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2170C>T
  hgvsp: ENSP00000403843.2:p.Arg724Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2170C>T
  hgvsp: ENSP00000432347.1:p.Arg724Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2170C>T
  hgvsp: ENSP00000271836.6:p.Arg724Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2170C>T
  hgvsp: ENSP00000349436.2:p.Arg724Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2170C>T
  hgvsp: ENSP00000348227.2:p.Arg724Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.449C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.456C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.41C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2170C>T
  hgvsp: ENSP00000352226.4:p.Arg724Ter
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg724Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-155032783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032783
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032783
    reference: chr 1
allele count: 4
allele frequency: 3.299948850792813e-5
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2171G>A
  hgvsp: ENSP00000352226.4:p.Arg724Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.457G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2171G>A
  hgvsp: ENSP00000353892.4:p.Arg724Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2207G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2171G>A
  hgvsp: ENSP00000271836.6:p.Arg724Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2171G>A
  hgvsp: ENSP00000432347.1:p.Arg724Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2171G>A
  hgvsp: ENSP00000348227.2:p.Arg724Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3817G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2171G>A
  hgvsp: ENSP00000434227.1:p.Arg724Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.211G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2171G>A
  hgvsp: ENSP00000349436.2:p.Arg724Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2201G>A
  hgvsp: ENSP00000432927.1:p.Arg734Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2171G>A
  hgvsp: ENSP00000403843.2:p.Arg724Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1289G>A
  hgvsp: ENSP00000357395.2:p.Arg430Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.254G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1289G>A
  hgvsp: ENSP00000357398.1:p.Arg430Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2171G>A
  hgvsp: ENSP00000357397.3:p.Arg724Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2301G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.450G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.42G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg724Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-155032785-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032785
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032785
    reference: chr 1
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2173C>T
  hgvsp: ENSP00000357397.3:p.Leu725Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.256C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1291C>T
  hgvsp: ENSP00000357395.2:p.Leu431Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2173C>T
  hgvsp: ENSP00000352226.4:p.Leu725Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2173C>T
  hgvsp: ENSP00000271836.6:p.Leu725Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2173C>T
  hgvsp: ENSP00000403843.2:p.Leu725Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2173C>T
  hgvsp: ENSP00000349436.2:p.Leu725Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2203C>T
  hgvsp: ENSP00000432927.1:p.Leu735Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3819C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1291C>T
  hgvsp: ENSP00000357398.1:p.Leu431Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.459C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2173C>T
  hgvsp: ENSP00000348227.2:p.Leu725Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2173C>T
  hgvsp: ENSP00000353892.4:p.Leu725Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2173C>T
  hgvsp: ENSP00000432347.1:p.Leu725Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2173C>T
  hgvsp: ENSP00000434227.1:p.Leu725Phe
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.44C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.452C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2303C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.213C>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2209C>T
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu725Phe
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/1-155032797-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032797
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032797
    reference: chr 1
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.268A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.471A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2185A>C
  hgvsp: ENSP00000352226.4:p.Lys729Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2185A>C
  hgvsp: ENSP00000432347.1:p.Lys729Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2185A>C
  hgvsp: ENSP00000348227.2:p.Lys729Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2185A>C
  hgvsp: ENSP00000349436.2:p.Lys729Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2185A>C
  hgvsp: ENSP00000357397.3:p.Lys729Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.56A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2185A>C
  hgvsp: ENSP00000353892.4:p.Lys729Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2185A>C
  hgvsp: ENSP00000271836.6:p.Lys729Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2185A>C
  hgvsp: ENSP00000434227.1:p.Lys729Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2215A>C
  hgvsp: ENSP00000432927.1:p.Lys739Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.464A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1303A>C
  hgvsp: ENSP00000357398.1:p.Lys435Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2185A>C
  hgvsp: ENSP00000403843.2:p.Lys729Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2315A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1303A>C
  hgvsp: ENSP00000357395.2:p.Lys435Gln
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3831A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2221A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.225A>C
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys729Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

1-155032798-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032798
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032797
    reference: chr 1
allele count: 1
allele frequency: 8.251097395953662e-6
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.229delG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2189delG
  hgvsp: ENSP00000271836.6:p.Gly730AspfsTer67
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2189delG
  hgvsp: ENSP00000353892.4:p.Gly730AspfsTer32
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2189delG
  hgvsp: ENSP00000403843.2:p.Gly730AspfsTer74
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2189delG
  hgvsp: ENSP00000352226.4:p.Gly730AspfsTer50
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2319delG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.468delG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2225delG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1307delG
  hgvsp: ENSP00000357398.1:p.Gly436AspfsTer67
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2189delG
  hgvsp: ENSP00000357397.3:p.Gly730AspfsTer8
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2189delG
  hgvsp: ENSP00000348227.2:p.Gly730AspfsTer92
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2189delG
  hgvsp: ENSP00000432347.1:p.Gly730AspfsTer75
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.475delG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2189delG
  hgvsp: ENSP00000349436.2:p.Gly730AspfsTer75
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.272delG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2189delG
  hgvsp: ENSP00000434227.1:p.Gly730AspfsTer50
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2219delG
  hgvsp: ENSP00000432927.1:p.Gly740AspfsTer67
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1307delG
  hgvsp: ENSP00000357395.2:p.Gly436AspfsTer67
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3835delG
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.60delG
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly730AspfsTer75
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: AG
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum

1-155032800-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032800
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032800
    reference: chr 1
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2188G>A
  hgvsp: ENSP00000348227.2:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2188G>A
  hgvsp: ENSP00000352226.4:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.228G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2188G>A
  hgvsp: ENSP00000353892.4:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1306G>A
  hgvsp: ENSP00000357398.1:p.Gly436Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2188G>A
  hgvsp: ENSP00000432347.1:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3834G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2188G>A
  hgvsp: ENSP00000403843.2:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2188G>A
  hgvsp: ENSP00000271836.6:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.59G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2188G>A
  hgvsp: ENSP00000357397.3:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1306G>A
  hgvsp: ENSP00000357395.2:p.Gly436Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2188G>A
  hgvsp: ENSP00000349436.2:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2224G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.467G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2218G>A
  hgvsp: ENSP00000432927.1:p.Gly740Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2188G>A
  hgvsp: ENSP00000434227.1:p.Gly730Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.271G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2318G>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.474G>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly730Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

1-155032800-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032800
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032800
    reference: chr 1
allele count: 2
allele frequency: 1.650192247396822e-5
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2188G>T
  hgvsp: ENSP00000432347.1:p.Gly730Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1306G>T
  hgvsp: ENSP00000357398.1:p.Gly436Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2318G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.474G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.271G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.228G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.59G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2188G>T
  hgvsp: ENSP00000352226.4:p.Gly730Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2188G>T
  hgvsp: ENSP00000348227.2:p.Gly730Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2224G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2188G>T
  hgvsp: ENSP00000271836.6:p.Gly730Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2188G>T
  hgvsp: ENSP00000357397.3:p.Gly730Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1306G>T
  hgvsp: ENSP00000357395.2:p.Gly436Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2188G>T
  hgvsp: ENSP00000353892.4:p.Gly730Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2218G>T
  hgvsp: ENSP00000432927.1:p.Gly740Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2188G>T
  hgvsp: ENSP00000434227.1:p.Gly730Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.467G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3834G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2188G>T
  hgvsp: ENSP00000349436.2:p.Gly730Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2188G>T
  hgvsp: ENSP00000403843.2:p.Gly730Ter
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly730Ter
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP

1-155032801-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032801
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032801
    reference: chr 1
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1307G>T
  hgvsp: ENSP00000357398.1:p.Gly436Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2189G>T
  hgvsp: ENSP00000349436.2:p.Gly730Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2189G>T
  hgvsp: ENSP00000432347.1:p.Gly730Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2225G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2189G>T
  hgvsp: ENSP00000357397.3:p.Gly730Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.468G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1307G>T
  hgvsp: ENSP00000357395.2:p.Gly436Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3835G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2189G>T
  hgvsp: ENSP00000434227.1:p.Gly730Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2319G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.475G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2189G>T
  hgvsp: ENSP00000353892.4:p.Gly730Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2189G>T
  hgvsp: ENSP00000403843.2:p.Gly730Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.272G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.60G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2189G>T
  hgvsp: ENSP00000352226.4:p.Gly730Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2219G>T
  hgvsp: ENSP00000432927.1:p.Gly740Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.229G>T
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2189G>T
  hgvsp: ENSP00000271836.6:p.Gly730Val
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2189G>T
  hgvsp: ENSP00000348227.2:p.Gly730Val
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly730Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/1-155032802-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032802
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032802
    reference: chr 1
allele count: 87
allele frequency: 7.281187754213883e-4
allele num: 119486
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2190A>C
  hgvsp: ENST00000356955.2:c.2190A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2190A>C
  hgvsp: ENST00000271836.6:c.2190A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2190A>C
  hgvsp: ENST00000368412.3:c.2190A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.230A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2190A>C
  hgvsp: ENST00000360674.4:c.2190A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2190A>C
  hgvsp: ENST00000449910.2:c.2190A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2190A>C
  hgvsp: ENST00000526491.1:c.2190A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1308A>C
  hgvsp: ENST00000368410.2:c.1308A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.469A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1308A>C
  hgvsp: ENST00000368413.1:c.1308A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2190A>C
  hgvsp: ENST00000529473.1:c.2190A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2220A>C
  hgvsp: ENST00000531455.1:c.2220A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2226A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2190A>C
  hgvsp: ENST00000355956.2:c.2190A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.61A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2190A>C
  hgvsp: ENST00000359280.4:c.2190A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.476A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2320A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3836A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.273A>C
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly730Gly
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/1-155032806-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032806
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032806
    reference: chr 1
allele count: 1015
allele frequency: 9.531053392679401e-3
allele num: 106494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.65A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2194A>C
  hgvsp: ENSP00000352226.4:p.Thr732Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1312A>C
  hgvsp: ENSP00000357395.2:p.Thr438Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2194A>C
  hgvsp: ENSP00000432347.1:p.Thr732Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2194A>C
  hgvsp: ENSP00000348227.2:p.Thr732Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2194A>C
  hgvsp: ENSP00000353892.4:p.Thr732Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2194A>C
  hgvsp: ENSP00000349436.2:p.Thr732Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2224A>C
  hgvsp: ENSP00000432927.1:p.Thr742Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.234A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.277A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2194A>C
  hgvsp: ENSP00000434227.1:p.Thr732Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.473A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2194A>C
  hgvsp: ENSP00000271836.6:p.Thr732Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.480A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1312A>C
  hgvsp: ENSP00000357398.1:p.Thr438Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2194A>C
  hgvsp: ENSP00000403843.2:p.Thr732Pro
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3840A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2230A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2324A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2194A>C
  hgvsp: ENSP00000357397.3:p.Thr732Pro
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr732Pro
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

http://identifiers.org/exac.variant/1-155032817-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032817
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032817
    reference: chr 1
allele count: 1
allele frequency: 8.257365570088519e-6
allele num: 121104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2205C>A
  hgvsp: ENSP00000432347.1:p.Tyr735Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.491C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.76C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.484C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2205C>A
  hgvsp: ENSP00000357397.3:p.Tyr735Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3851C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2205C>A
  hgvsp: ENSP00000353892.4:p.Tyr735Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1323C>A
  hgvsp: ENSP00000357398.1:p.Tyr441Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1323C>A
  hgvsp: ENSP00000357395.2:p.Tyr441Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2205C>A
  hgvsp: ENSP00000403843.2:p.Tyr735Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2205C>A
  hgvsp: ENSP00000352226.4:p.Tyr735Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2205C>A
  hgvsp: ENSP00000349436.2:p.Tyr735Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2205C>A
  hgvsp: ENSP00000271836.6:p.Tyr735Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.245C>A
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2235C>A
  hgvsp: ENSP00000432927.1:p.Tyr745Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2205C>A
  hgvsp: ENSP00000434227.1:p.Tyr735Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2205C>A
  hgvsp: ENSP00000348227.2:p.Tyr735Ter
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.288C>A
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Tyr735Ter
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/1-155032818-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032818
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032818
    reference: chr 1
allele count: 14
allele frequency: 1.155973908017505e-4
allele num: 121110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1324A>C
  hgvsp: ENST00000368413.1:c.1324A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.246A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1324A>C
  hgvsp: ENST00000368410.2:c.1324A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2206A>C
  hgvsp: ENST00000449910.2:c.2206A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2206A>C
  hgvsp: ENST00000529473.1:c.2206A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2236A>C
  hgvsp: ENST00000531455.1:c.2236A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2206A>C
  hgvsp: ENST00000368412.3:c.2206A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2206A>C
  hgvsp: ENSP00000353892.4:p.Ser736Arg
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2206A>C
  hgvsp: ENST00000271836.6:c.2206A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.289A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2206A>C
  hgvsp: ENST00000356955.2:c.2206A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.77A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2336A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2206A>C
  hgvsp: ENST00000355956.2:c.2206A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.485A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3852A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.492A>C
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2206A>C
  hgvsp: ENST00000359280.4:c.2206A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/193
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser736Arg
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

1-155032828-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032828
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032828
    reference: chr 1
allele count: 1
allele frequency: 8.265555775970376e-6
allele num: 120984
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1325+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1325+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2207+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2207+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2337+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2237+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.78+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2207+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.247+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.493+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3853+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.486+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2207+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.290+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2207+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2243+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2207+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2207+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2207+9A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2207+9A>G
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3759
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-155032836-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032836
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032836
    reference: chr 1
allele count: 1
allele frequency: 8.274309922552459e-6
allele num: 120856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3853+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2207+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.290+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2207+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2243+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.493+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.247+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2207+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1325+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2207+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.78+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.486+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1325+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2207+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2207+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2207+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2337+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2237+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2207+17C>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2207+17C>G
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

1-155032842-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 155032842
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 155032842
    reference: chr 1
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000472434
  gene symbol: ADAM15
  hgvsc: ENST00000472434.1:n.2243+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000352226
  ensembl transcript: ENST00000359280
  gene symbol: ADAM15
  hgvsc: ENST00000359280.4:c.2207+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461234
  gene symbol: ADAM15
  hgvsc: ENST00000461234.1:n.486+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000434227
  ensembl transcript: ENST00000529473
  gene symbol: ADAM15
  hgvsc: ENST00000529473.1:c.2207+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000353892
  ensembl transcript: ENST00000360674
  gene symbol: ADAM15
  hgvsc: ENST00000360674.4:c.2207+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000468053
  gene symbol: ADAM15
  hgvsc: ENST00000468053.1:n.78+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000461564
  gene symbol: ADAM15
  hgvsc: ENST00000461564.2:n.2337+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000474709
  gene symbol: ADAM15
  hgvsc: ENST00000474709.1:n.290+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357398
  ensembl transcript: ENST00000368413
  gene symbol: ADAM15
  hgvsc: ENST00000368413.1:c.1325+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000498481
  gene symbol: ADAM15
  hgvsc: ENST00000498481.2:n.493+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432347
  ensembl transcript: ENST00000526491
  gene symbol: ADAM15
  hgvsc: ENST00000526491.1:c.2207+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000349436
  ensembl transcript: ENST00000356955
  gene symbol: ADAM15
  hgvsc: ENST00000356955.2:c.2207+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000462116
  gene symbol: ADAM15
  hgvsc: ENST00000462116.1:n.247+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357397
  ensembl transcript: ENST00000368412
  gene symbol: ADAM15
  hgvsc: ENST00000368412.3:c.2207+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000348227
  ensembl transcript: ENST00000355956
  gene symbol: ADAM15
  hgvsc: ENST00000355956.2:c.2207+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000432927
  ensembl transcript: ENST00000531455
  gene symbol: ADAM15
  hgvsc: ENST00000531455.1:c.2237+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000357395
  ensembl transcript: ENST00000368410
  gene symbol: ADAM15
  hgvsc: ENST00000368410.2:c.1325+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000271836
  ensembl transcript: ENST00000271836
  gene symbol: ADAM15
  hgvsc: ENST00000271836.6:c.2207+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl protein: ENSP00000403843
  ensembl transcript: ENST00000449910
  gene symbol: ADAM15
  hgvsc: ENST00000449910.2:c.2207+23A>G
  variant of: http://identifiers.org/hgnc/193
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143537
  ensembl transcript: ENST00000527418
  gene symbol: ADAM15
  hgvsc: ENST00000527418.1:n.3853+23A>G
  variant of: http://identifiers.org/hgnc/193
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 1950
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2106
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1454
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3378
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4627
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2790
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3701
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4904
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4028
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2866
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1662
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3608
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4921
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9766
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 923
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1787
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47955
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
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: 906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.158779e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.136e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

QD
type: SiteQuality
SIO_000300: 1.506e1

MQ
type: SiteQuality
SIO_000300: 5.999e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

GenotypeDepth
all individuals: 1950
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1662
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4904
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1454
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4028
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3378
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3701
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4921
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2866
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 9766
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2790
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3608
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4627
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2106
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4171
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6504
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1787
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 923
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47955
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
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: 906
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.136e0

DP
type: SiteQuality
SIO_000300: 4.158779e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

QD
type: SiteQuality
SIO_000300: 1.506e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.999e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

VQSLOD
type: SiteQuality
SIO_000300: 4.28e0

GenotypeDepth
all individuals: 1659
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 258
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4627
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2107
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3608
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3700
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2867
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4026
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1912
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3315
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9763
bin: 9.75e1
variant carriers: 12

GenotypeDepth
all individuals: 4922
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2790
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4904
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1443
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 921
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1761
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47956
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6419
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 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: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 13
allele frequency: 1.504281416338811e-3
allele num: 8642
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.157583e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 9.01e-1

QD
type: SiteQuality
SIO_000300: 9.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.898e0

FS
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.98e-1

GenotypeDepth
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9756
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1658
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2868
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4627
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4025
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2107
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 275
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1434
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4921
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1888
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4173
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3307
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3608
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3700
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4906
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2793
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 235
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6364
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1739
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47954
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 2
allele frequency: 3.004446580939791e-5
allele num: 66568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

QD
type: SiteQuality
SIO_000300: 1.19e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

DP
type: SiteQuality
SIO_000300: 4.154805e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.854e0

GenotypeDepth
all individuals: 121
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1867
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2867
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4027
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4173
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4626
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2107
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 307
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4921
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3273
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2793
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3608
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9756
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4907
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1659
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3700
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1425
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6361
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 920
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47953
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1736
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 66550
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.284e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

FS
type: SiteQuality
SIO_000300: 1.451e0

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

MQRankSum
type: SiteQuality
SIO_000300: 2.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.18e0

DP
type: SiteQuality
SIO_000300: 4.153419e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000143537
ensembl transcript: ENST00000461564
gene symbol: ADAM15
hgvsc: ENST00000461564.2:n.2198G>C
variant of: http://identifiers.org/hgnc/193

GenotypeDepth
all individuals: 2867
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4173
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3098
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 447
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2106
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1804
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4907
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 351
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1656
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3952
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2793
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3608
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1423
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3700
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4921
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4626
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9755
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4369
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 521
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 163
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47951
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5957
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503895088278642e-5
allele num: 66494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 10368
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.870000000000001e-1

DP
type: SiteQuality
SIO_000300: 4.149182e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.643e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

MQRankSum
type: SiteQuality
SIO_000300: -4.85e-1

QD
type: SiteQuality
SIO_000300: 1.096e1

VQSLOD
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

FS
type: SiteQuality
SIO_000300: 2.652e0

GenotypeDepth
all individuals: 3608
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4921
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4626
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 495
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2105
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 370
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3927
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2867
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1658
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 162
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9755
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2793
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3101
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4907
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1402
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4173
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1765
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4368
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3700
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 2.25e1
variant carriers: 0

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

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

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

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

East Asian
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Other
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European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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African
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allele frequency: 5.79598145285935e-4
allele num: 10352
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Latino
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MQRankSum
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SIO_000300: -3.9e-2

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

East Asian
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Latino
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African
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Other
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South Asian
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European (Non-Finnish)
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allele frequency: 6.037553583288052e-5
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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South Asian
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European (Non-Finnish)
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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allele num: 66240
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South Asian
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Other
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MQ
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QD
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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European (Non-Finnish)
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African
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South Asian
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East Asian
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European (Finnish)
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MQRankSum
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DP
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BaseQRankSum
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FS
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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African
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European (Non-Finnish)
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East Asian
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Other
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South Asian
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QD
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MQ
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 1.505525277769414e-5
allele num: 66422
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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MQRankSum
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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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VQSLOD
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503126503126503e-5
allele num: 66528
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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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European (Finnish)
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Latino
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QD
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.927153594141453e-4
allele num: 10378
num of homozygotes: 0

European (Finnish)
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allele frequency: 8.015728977616455e-3
allele num: 6612
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European (Non-Finnish)
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allele frequency: 5.15448425102188e-3
allele num: 66544
num of homozygotes: 0

South Asian
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allele frequency: 1.160943419283881e-3
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East Asian
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allele num: 8654
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Latino
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Other
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FS
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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DP
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MQRankSum
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
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num of homozygotes: 0

South Asian
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allele num: 16318
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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African
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East Asian
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QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 4
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allele num: 66548
num of homozygotes: 0

African
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East Asian
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Other
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MQ
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SIO_000300: 5.973e1

ClippingRankSum
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MQRankSum
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DP
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ReadPosRankSum
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QD
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FS
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 0.0e0
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 1197

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 6
allele frequency: 6.651884700665188e-3
allele num: 902
num of homozygotes: 0

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

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

South Asian
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allele count: 4
allele frequency: 2.42306760358614e-4
allele num: 16508
num of homozygotes: 0

Latino
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allele count: 48
allele frequency: 4.158004158004158e-3
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.650957555382122e-4
allele num: 66628
num of homozygotes: 0

African
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allele count: 1236
allele frequency: 1.19212962962963e-1
allele num: 10368
num of homozygotes: 82

MQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

VQSLOD
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SIO_000300: 3.36e0

FS
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BaseQRankSum
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SIO_000300: -1.577e0

InbreedingCoeff
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SIO_000300: 1.01e-1

QD
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SIO_000300: 1.352e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 2.16937e6

GenotypeDepth
all individuals: 84
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

GenotypeQuality
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GenotypeQuality
all individuals: 5338
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.268e-1

ClippingRankSum
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SIO_000300: -2.1e-1

BaseQRankSum
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SIO_000300: 4.65e0

MQRankSum
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SIO_000300: -5.7e-1

ReadPosRankSum
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SIO_000300: -9.0e-2

FS
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SIO_000300: 1.0201e1

DP
type: SiteQuality
SIO_000300: 2.151759e6

InbreedingCoeff
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SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
SIO_000300: 1.47e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13858
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variant carriers: 1

GenotypeQuality
all individuals: 7858
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.152376e6

FS
type: SiteQuality
SIO_000300: 2.723e0

QD
type: SiteQuality
SIO_000300: 3.015e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.899e1

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.611e0

BaseQRankSum
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SIO_000300: -3.287e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.506e0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 101
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variant carriers: 0

GenotypeDepth
all individuals: 576
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variant carriers: 0

GenotypeDepth
all individuals: 2415
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 202
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GenotypeDepth
all individuals: 199
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 87
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 229
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2491
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 2.0e-4

ReadPosRankSum
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VQSLOD
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SIO_000300: -9.983e-1

MQRankSum
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ClippingRankSum
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QD
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SIO_000300: 2.031e1

DP
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SIO_000300: 2.151217e6

FS
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SIO_000300: 3.464e0

MQ
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SIO_000300: 5.935e1

BaseQRankSum
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SIO_000300: 1.12e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.50355781067043e-5
allele num: 66614
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 2
allele frequency: 1.732201628269531e-4
allele num: 11546
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
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QD
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SIO_000300: 1.194e1

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

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

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

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3547
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13898
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8044
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.335e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.92e-2

QD
type: SiteQuality
SIO_000300: 2.534e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.151623e6

GenotypeDepth
all individuals: 9428
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4076
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 279
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 850
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1447
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14353
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12995
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2399
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 322
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6673
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 197
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6204
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 147
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17372
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4640
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2513
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3982
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13884
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
SIO_000300: 5.384e1

DP
type: SiteQuality
SIO_000300: 2.151407e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.387e0

MQRankSum
type: SiteQuality
SIO_000300: -1.041e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.207e0

QD
type: SiteQuality
SIO_000300: 4.51e0

GenotypeDepth
all individuals: 280
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 8.75e1
variant carriers: 5

GenotypeDepth
all individuals: 9473
bin: 3.75e1
variant carriers: 10

GenotypeDepth
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 857
bin: 6.25e1
variant carriers: 9

GenotypeDepth
all individuals: 534
bin: 6.75e1
variant carriers: 7

GenotypeDepth
all individuals: 376
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6140
bin: 2.25e1
variant carriers: 4

GenotypeDepth
all individuals: 12987
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14212
bin: 2.75e1
variant carriers: 3

GenotypeDepth
all individuals: 2392
bin: 5.25e1
variant carriers: 8

GenotypeDepth
all individuals: 6712
bin: 4.25e1
variant carriers: 8

GenotypeDepth
all individuals: 1470
bin: 5.75e1
variant carriers: 8

GenotypeDepth
all individuals: 207
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 4097
bin: 4.75e1
variant carriers: 3

GenotypeDepth
all individuals: 98
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 336
bin: 7.25e1
variant carriers: 8

GenotypeDepth
all individuals: 199
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 163
bin: 8.25e1
variant carriers: 7

GenotypeDepth
all individuals: 62
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4489
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 290
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 104
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 365
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 347
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7708
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 122
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 282
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3440
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2427
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16768
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5152
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3818
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 13328
bin: 9.75e1
variant carriers: 72

South Asian
type: Population
allele count: 2
allele frequency: 1.21300339640951e-4
allele num: 16488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 14
allele frequency: 2.273465410847678e-3
allele num: 6158
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.735809755250825e-4
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.973500697350069e-4
allele num: 8604
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.912897491605768e-4
allele num: 10126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 56
allele frequency: 8.520220308553693e-4
allele num: 65726
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

DP
type: SiteQuality
SIO_000300: 2.156258e6

VQSLOD
type: SiteQuality
SIO_000300: -7.479000000000001e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 1.24143e2

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.956e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.431e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.9e0

QD
type: SiteQuality
SIO_000300: 4.83e0

GenotypeDepth
all individuals: 630
bin: 7.25e1
variant carriers: 59

GenotypeDepth
all individuals: 2695
bin: 5.25e1
variant carriers: 72

GenotypeDepth
all individuals: 218
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 294
bin: 1.75e1
variant carriers: 5

GenotypeDepth
all individuals: 5523
bin: 2.25e1
variant carriers: 13

GenotypeDepth
all individuals: 9029
bin: 3.75e1
variant carriers: 35

GenotypeDepth
all individuals: 199
bin: 9.25e1
variant carriers: 56

GenotypeDepth
all individuals: 6574
bin: 4.25e1
variant carriers: 45

GenotypeDepth
all individuals: 4189
bin: 4.75e1
variant carriers: 52

GenotypeDepth
all individuals: 856
bin: 6.75e1
variant carriers: 59

GenotypeDepth
all individuals: 1163
bin: 6.25e1
variant carriers: 77

GenotypeDepth
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1685
bin: 5.75e1
variant carriers: 63

GenotypeDepth
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 348
bin: 8.25e1
variant carriers: 58

GenotypeDepth
all individuals: 492
bin: 7.75e1
variant carriers: 56

GenotypeDepth
all individuals: 268
bin: 8.75e1
variant carriers: 61

GenotypeDepth
all individuals: 776
bin: 9.75e1
variant carriers: 320

GenotypeDepth
all individuals: 13362
bin: 2.75e1
variant carriers: 16

GenotypeDepth
all individuals: 12286
bin: 3.25e1
variant carriers: 21

GenotypeQuality
all individuals: 6795
bin: 6.75e1
variant carriers: 23

GenotypeQuality
all individuals: 570
bin: 4.75e1
variant carriers: 20

GenotypeQuality
all individuals: 517
bin: 3.75e1
variant carriers: 27

GenotypeQuality
all individuals: 293
bin: 1.25e1
variant carriers: 16

GenotypeQuality
all individuals: 6513
bin: 2.5e0
variant carriers: 7

GenotypeQuality
all individuals: 696
bin: 5.75e1
variant carriers: 35

GenotypeQuality
all individuals: 674
bin: 5.25e1
variant carriers: 29

GenotypeQuality
all individuals: 2897
bin: 9.25e1
variant carriers: 23

GenotypeQuality
all individuals: 559
bin: 4.25e1
variant carriers: 31

GenotypeQuality
all individuals: 262
bin: 7.5e0
variant carriers: 15

GenotypeQuality
all individuals: 1986
bin: 8.75e1
variant carriers: 26

GenotypeQuality
all individuals: 481
bin: 2.25e1
variant carriers: 17

GenotypeQuality
all individuals: 286
bin: 1.75e1
variant carriers: 16

GenotypeQuality
all individuals: 416
bin: 2.75e1
variant carriers: 28

GenotypeQuality
all individuals: 15407
bin: 6.25e1
variant carriers: 18

GenotypeQuality
all individuals: 10367
bin: 9.75e1
variant carriers: 637

GenotypeQuality
all individuals: 3208
bin: 7.25e1
variant carriers: 30

GenotypeQuality
all individuals: 4428
bin: 7.75e1
variant carriers: 22

GenotypeQuality
all individuals: 459
bin: 3.25e1
variant carriers: 25

GenotypeQuality
all individuals: 3855
bin: 8.25e1
variant carriers: 24

South Asian
type: Population
allele count: 21
allele frequency: 1.291830708661417e-3
allele num: 16256
num of homozygotes: 0

African
type: Population
allele count: 161
allele frequency: 2.019568489713999e-2
allele num: 7972
num of homozygotes: 0

East Asian
type: Population
allele count: 91
allele frequency: 1.128192412596082e-2
allele num: 8066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 67
allele frequency: 1.394090719933417e-2
allele num: 4806
num of homozygotes: 0

Latino
type: Population
allele count: 40
allele frequency: 3.693444136657433e-3
allele num: 10830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 627
allele frequency: 1.084137358647163e-2
allele num: 57834
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 1.095890410958904e-2
allele num: 730
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.991e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.868e0

QD
type: SiteQuality
SIO_000300: 2.31e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.584e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.31e0

DP
type: SiteQuality
SIO_000300: 2.2997e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.58e-2

FS
type: SiteQuality
SIO_000300: 2.522e2

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000143537
ensembl transcript: ENST00000472434
gene symbol: ADAM15
hgvsc: ENST00000472434.1:n.2241C>A
variant of: http://identifiers.org/hgnc/193

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000143537
ensembl transcript: ENST00000461564
gene symbol: ADAM15
hgvsc: ENST00000461564.2:n.2335C>A
variant of: http://identifiers.org/hgnc/193

GenotypeDepth
all individuals: 663
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2142
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 225
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5735
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 132
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 347
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 242
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15813
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13850
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6349
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1218
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 115
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9312
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3765
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12415
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4612
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8418
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19319
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 354
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3816
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5351
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.082725060827251e-5
allele num: 16440
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.324e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.13e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.287e-1

QD
type: SiteQuality
SIO_000300: 6.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.55e-1

DP
type: SiteQuality
SIO_000300: 2.100926e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000143537
ensembl transcript: ENST00000472434
gene symbol: ADAM15
hgvsc: ENST00000472434.1:n.2242A>C
variant of: http://identifiers.org/hgnc/193

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000143537
ensembl protein: ENSP00000432347
ensembl transcript: ENST00000526491
gene symbol: ADAM15
hgvsc: ENST00000526491.1:c.2206A>C
hgvsp: ENST00000526491.1:c.2206A>C(p.%3D)
variant of: http://identifiers.org/hgnc/193

GenotypeDepth
all individuals: 1216
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 141
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9306
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 15825
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 222
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 402
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 664
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 46
bin: 9.25e1
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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African
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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DP
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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African
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South Asian
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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MQ
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ClippingRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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Latino
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European (Non-Finnish)
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Other
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South Asian
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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