ClinVar Miner

List of variants in gene combination CARD14, SGSH reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001366385.1(CARD14):c.2807+248T>C rs6565646 0.68300
NM_001366385.1(CARD14):c.1852-60T>C rs2304856 0.51286
NM_001366385.1(CARD14):c.2692-151A>C rs4889998 0.48278
NM_001366385.1(CARD14):c.*288G>A rs7211773 0.47806
NM_001366385.1(CARD14):c.*274G>A rs7211656 0.47804
NM_001366385.1(CARD14):c.2808-252A>G rs7210317 0.47803
NM_001366385.1(CARD14):c.2692-182A>G rs4889837 0.47475
NM_001366385.1(CARD14):c.2808-290C>T rs7222024 0.47387
NM_001366385.1(CARD14):c.2398+42T>C rs4889836 0.41735
NM_001366385.1(CARD14):c.2398+30A>G rs4889996 0.41701
NM_001366385.1(CARD14):c.2219+252T>C rs11150848 0.41494
NM_001366385.1(CARD14):c.2398+49G>A rs4889997 0.40159
NM_001366385.1(CARD14):c.1979-125C>A rs3813063 0.39784
NM_001366385.1(CARD14):c.2398+220T>C rs9914039 0.07405
NM_001366385.1(CARD14):c.2219+258C>G rs9914128 0.07362
NM_001366385.1(CARD14):c.2283+11A>C rs9905662 0.07362
NM_001366385.1(CARD14):c.*231T>G rs9890208 0.05755
NM_001366385.1(CARD14):c.2807+123C>T rs62074416 0.05669
NM_001366385.1(CARD14):c.2885G>A (p.Arg962Gln) rs34850974 0.04584
NM_001366385.1(CARD14):c.2853G>A (p.Glu951=) rs78569961 0.01590
NM_001366385.1(CARD14):c.2044C>T (p.Arg682Trp) rs117918077 0.01097
NM_001366385.1(CARD14):c.2267G>A (p.Cys756Tyr) rs34822755 0.01019
NM_001366385.1(CARD14):c.*7G>A rs114706038 0.00912
NM_001366385.1(CARD14):c.2193G>A (p.Ala731=) rs35692270 0.00788
NM_001366385.1(CARD14):c.2772C>T (p.His924=) rs146356100 0.00593
NM_001366385.1(CARD14):c.2763C>T (p.Ile921=) rs150378107 0.00572
NM_001366385.1(CARD14):c.2829C>T (p.Gly943=) rs200640336 0.00496
NM_001366385.1(CARD14):c.2822G>A (p.Arg941Gln) rs74000616 0.00421
NM_001366385.1(CARD14):c.2859G>A (p.Ala953=) rs139969019 0.00386
NM_001366385.1(CARD14):c.1917C>T (p.Ala639=) rs79407194 0.00344
NM_001366385.1(CARD14):c.1979-15G>A rs199898989 0.00303
NM_001366385.1(CARD14):c.2335G>A (p.Ala779Thr) rs141913003 0.00220
NM_001366385.1(CARD14):c.1852-16C>T rs186883652 0.00139
NM_001366385.1(CARD14):c.2140G>A (p.Gly714Ser) rs151150961 0.00035
NM_001366385.1(CARD14):c.1852-8G>A rs544120287 0.00023
NM_001366385.1(CARD14):c.2807+10C>T rs368700533 0.00019
NM_001366385.1(CARD14):c.2398+14A>C rs573376427 0.00003
NM_001366385.1(CARD14):c.2775C>T (p.Val925=) rs372790630 0.00003
NM_001366385.1(CARD14):c.1998G>A (p.Gln666=) rs142087113 0.00002
NM_001366385.1(CARD14):c.1852-303TTTCT[5] rs3217504
NM_001366385.1(CARD14):c.1978+142del rs11356264
NM_001366385.1(CARD14):c.2219+14T>A rs8069255
NM_001366385.1(CARD14):c.2219+14T>G rs8069255
NM_001366385.1(CARD14):c.2219+277G>C rs11150849
NM_001366385.1(CARD14):c.2283+121C>G rs2289540
NM_001366385.1(CARD14):c.2807+233G>A rs7221289
NM_001366385.1(CARD14):c.2808-19C>A rs111745899
NM_001366385.1(CARD14):c.2808-19C>G rs111745899
NM_001366385.1(CARD14):c.2808-20C>A rs545159633
NM_001366385.1(CARD14):c.2919C>G (p.Asp973Glu) rs144285237

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.