ClinVar Miner

List of variants in gene CYP17A1 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000102.4(CYP17A1):c.1244-223T>C rs284850 0.99955
NM_000102.4(CYP17A1):c.195G>T (p.Ser65=) rs6163 0.40112
NM_000102.4(CYP17A1):c.138C>T (p.His46=) rs6162 0.40089
NM_000102.4(CYP17A1):c.969+75C>G rs3740397 0.35372
NM_000102.4(CYP17A1):c.436+105A>C rs743575 0.24877
NM_000102.4(CYP17A1):c.1243+113A>T rs10883783 0.24865
NM_000102.4(CYP17A1):c.298-99C>T rs4919687 0.24836
NM_000102.4(CYP17A1):c.1139+19T>G rs4919686 0.21485
NM_000102.4(CYP17A1):c.1139+143C>T rs284848 0.15814
NM_000102.4(CYP17A1):c.1243+83C>A rs284849 0.15759
NM_000102.4(CYP17A1):c.666+35T>C rs1004467 0.13602
NM_000102.4(CYP17A1):c.1140-25C>A rs17115100 0.09902
NM_000102.4(CYP17A1):c.666+141A>T rs17115104 0.03467
NM_000102.4(CYP17A1):c.437-83C>T rs755443 0.03156
NM_000102.4(CYP17A1):c.1244-228T>C rs11191413 0.03120
NM_000102.4(CYP17A1):c.1140-271C>T rs45609333 0.01681
NM_000102.4(CYP17A1):c.437-57A>G rs45583734 0.00452
NM_000102.4(CYP17A1):c.437-52G>A rs71471253 0.00125
NM_000102.4(CYP17A1):c.436+80A>G rs61754272 0.00081
NM_000102.4(CYP17A1):c.970-18A>G rs61754277 0.00062
NM_000102.4(CYP17A1):c.1139+79C>T rs45504696
NM_000102.4(CYP17A1):c.1244-129_1244-95del rs139275291
NM_000102.4(CYP17A1):c.298-271A>C rs3781287
NM_000102.4(CYP17A1):c.754-251del rs1177497362
NM_000102.4(CYP17A1):c.969+13dup

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.