ClinVar Miner

List of variants in gene CLIC5 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_016929.5(CLIC5):c.173+23G>A rs3734206 0.84107
NM_001114086.2(CLIC5):c.540+291A>G rs9472684 0.28890
NM_001114086.2(CLIC5):c.541-60702G>C rs9472663 0.23905
NM_016929.5(CLIC5):c.63+241T>C rs9472662 0.19955
NM_016929.5(CLIC5):c.588+1654A>G rs6458477 0.18738
NM_001114086.2(CLIC5):c.540+306G>A rs9369596 0.16741
NM_001114086.2(CLIC5):c.540+300A>G rs9381422 0.16737
NM_001114086.2(CLIC5):c.540+171A>G rs9381423 0.16581
NM_001114086.2(CLIC5):c.522G>A (p.Glu174=) rs3734207 0.12968
NM_016929.5(CLIC5):c.174-23C>A rs56131491 0.05892
NM_001370649.1(CLIC5):c.-55+49000C>A rs6909590 0.04698
NM_001114086.2(CLIC5):c.340A>G (p.Thr114Ala) rs723580 0.04335
NM_001370649.1(CLIC5):c.-55+49121C>A rs35067690 0.03641
NM_016929.5(CLIC5):c.173+76C>T rs74786400 0.02280
NM_016929.5(CLIC5):c.588+1480T>C rs75878754 0.01849
NM_016929.5(CLIC5):c.293C>A (p.Pro98His) rs35822882 0.01752
NM_016929.5(CLIC5):c.300-20C>T rs140116349 0.00712
NM_016929.5(CLIC5):c.588+1486T>C rs75780343 0.00605
NM_001114086.2(CLIC5):c.10G>A (p.Glu4Lys) rs116755302 0.00545
NM_001114086.2(CLIC5):c.237A>T (p.Arg79Ser) rs41271277 0.00309
NM_016929.5(CLIC5):c.341C>A (p.Ala114Glu) rs143360018 0.00200
NM_016929.5(CLIC5):c.508G>C (p.Gly170Arg) rs114149334 0.00181
NM_001114086.2(CLIC5):c.117C>T (p.Tyr39=) rs138306261 0.00153
NM_016929.5(CLIC5):c.477G>T (p.Glu159Asp) rs148377014 0.00150
NM_016929.5(CLIC5):c.326G>A (p.Arg109Gln) rs117204561 0.00116
NM_016929.5(CLIC5):c.515G>A (p.Arg172Gln) rs145681060 0.00103
NM_016929.5(CLIC5):c.73G>A (p.Asp25Asn) rs145250435 0.00091
NM_001114086.2(CLIC5):c.299A>T (p.Gln100Leu) rs74387983 0.00069
NM_016929.5(CLIC5):c.425C>T (p.Thr142Ile) rs141036777 0.00047
NM_016929.5(CLIC5):c.491C>G (p.Thr164Ser) rs201781198 0.00025
NM_016929.5(CLIC5):c.696A>T (p.Ala232=) rs187897856 0.00025
NM_001114086.2(CLIC5):c.363A>G (p.Ala121=) rs1010510364
NM_016929.5(CLIC5):c.-287G>T rs116332814
NM_016929.5(CLIC5):c.406+139dup rs11421773
NM_016929.5(CLIC5):c.589-9_589-8del rs3831297
NM_016929.5(CLIC5):c.63+141C>G rs115982120
NM_016929.5(CLIC5):c.64-145T>G rs6909306

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.