ClinVar Miner

List of variants in gene CYP17A1 reported by OMIM

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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_000102.4(CYP17A1):c.286C>T (p.Arg96Trp) rs104894138 0.00006
NM_000102.4(CYP17A1):c.374G>A (p.Arg125Gln) rs104894154 0.00003
NM_000102.4(CYP17A1):c.1247G>A (p.Arg416His) rs104894155 0.00002
NM_000102.4(CYP17A1):c.1040G>A (p.Arg347His) rs61754278 0.00001
NM_000102.4(CYP17A1):c.1073G>A (p.Arg358Gln) rs104894139 0.00001
NM_000102.4(CYP17A1):c.1084C>T (p.Arg362Cys) rs104894142 0.00001
NM_000102.4(CYP17A1):c.1216T>C (p.Trp406Arg) rs104894143 0.00001
NM_000102.4(CYP17A1):c.287G>A (p.Arg96Gln) rs104894153 0.00001
NM_000102.4(CYP17A1):c.316T>C (p.Ser106Pro) rs104894135 0.00001
NG_007955.1:g.7152_7674delins469
NM_000102.4(CYP17A1):c.1024C>A (p.Pro342Thr) rs104894137
NM_000102.4(CYP17A1):c.1039C>T (p.Arg347Cys) rs104894149
NM_000102.4(CYP17A1):c.1243+5G>A rs1564777724
NM_000102.4(CYP17A1):c.1283C>T (p.Pro428Leu) rs104894145
NM_000102.4(CYP17A1):c.1313del (p.Gly438fs) rs2134081192
NM_000102.4(CYP17A1):c.1358T>C (p.Phe453Ser) rs104894151
NM_000102.4(CYP17A1):c.1435_1438dup (p.Pro480fs) rs556794126
NM_000102.4(CYP17A1):c.1459_1467del (p.Asp487_Phe489del) rs756135168
NM_000102.4(CYP17A1):c.157TTC[1] (p.Phe54del) rs121434319
NM_000102.4(CYP17A1):c.206_230del (p.Gly69fs) rs786205062
NM_000102.4(CYP17A1):c.278T>G (p.Phe93Cys) rs104894146
NM_000102.4(CYP17A1):c.340T>G (p.Phe114Val) rs104894147
NM_000102.4(CYP17A1):c.347A>T (p.Asp116Val) rs104894148
NM_000102.4(CYP17A1):c.353_359dup (p.His120fs) rs1844147475
NM_000102.4(CYP17A1):c.436+5G>T rs786205061
NM_000102.4(CYP17A1):c.437-2A>C rs1395913655
NM_000102.4(CYP17A1):c.51G>A (p.Trp17Ter) rs104894141
NM_000102.4(CYP17A1):c.601T>A (p.Tyr201Asn) rs104894150
NM_000102.4(CYP17A1):c.667-13_667-10del rs1844127277
NM_000102.4(CYP17A1):c.715C>T (p.Arg239Ter) rs104894136
NM_000102.4(CYP17A1):c.81C>A (p.Tyr27Ter) rs104894152
NM_000102.4(CYP17A1):c.985T>G (p.Tyr329Asp) rs104894144

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