ClinVar Miner

List of variants in gene CAPN3 reported as likely benign

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Total variants: 63
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HGVS dbSNP
NM_000070.2(CAPN3):c.-25G>C rs1405523432
NM_000070.2(CAPN3):c.1017G>A (p.Thr339=) rs141934227
NM_000070.2(CAPN3):c.1020G>T (p.Gly340=) rs372401631
NM_000070.2(CAPN3):c.1029+3A>G rs28364442
NM_000070.2(CAPN3):c.1194-18_1194-17delCT rs367976885
NM_000070.2(CAPN3):c.1227A>C (p.Thr409=) rs111806046
NM_000070.2(CAPN3):c.1227A>G (p.Thr409=) rs111806046
NM_000070.2(CAPN3):c.1263G>A (p.Leu421=) rs372450879
NM_000070.2(CAPN3):c.1302C>T (p.Asn434=) rs751429914
NM_000070.2(CAPN3):c.1308C>T (p.Gly436=) rs372968945
NM_000070.2(CAPN3):c.1350C>T (p.Phe450=) rs144944366
NM_000070.2(CAPN3):c.1355-6G>A rs28364485
NM_000070.2(CAPN3):c.1410C>T (p.Asp470=) rs371148431
NM_000070.2(CAPN3):c.1525-16T>G rs1555422168
NM_000070.2(CAPN3):c.1543G>A (p.Gly515Arg) rs150226817
NM_000070.2(CAPN3):c.1584C>T (p.Asn528=) rs530529988
NM_000070.2(CAPN3):c.1668C>T (p.Ile556=) rs199884116
NM_000070.2(CAPN3):c.1746-20C>G rs201892814
NM_000070.2(CAPN3):c.1746-7C>G rs199978708
NM_000070.2(CAPN3):c.1800+12G>A rs542523863
NM_000070.2(CAPN3):c.1818G>A (p.Ser606=) rs28364528
NM_000070.2(CAPN3):c.1830C>T (p.Asn610=) rs202019404
NM_000070.2(CAPN3):c.183C>T (p.Phe61=) rs146069933
NM_000070.2(CAPN3):c.1914+13G>C rs769337232
NM_000070.2(CAPN3):c.2051-11C>T rs886038224
NM_000070.2(CAPN3):c.2071G>A (p.Gly691Arg) rs140425651
NM_000070.2(CAPN3):c.2079A>G (p.Thr693=) rs540561728
NM_000070.2(CAPN3):c.2088C>A (p.Ser696=) rs867628179
NM_000070.2(CAPN3):c.2088C>T (p.Ser696=) rs867628179
NM_000070.2(CAPN3):c.2109C>T (p.Leu703=) rs371577901
NM_000070.2(CAPN3):c.2154C>T (p.His718=) rs1351586112
NM_000070.2(CAPN3):c.2235C>T (p.Tyr745=) rs147774793
NM_000070.2(CAPN3):c.2263+14A>G rs886038225
NM_000070.2(CAPN3):c.2264-11C>T rs28364537
NM_000070.2(CAPN3):c.2292C>T (p.Asp764=) rs187279903
NM_000070.2(CAPN3):c.232C>A (p.Pro78Thr) rs138867099
NM_000070.2(CAPN3):c.2332G>A (p.Asp778Asn) rs115311625
NM_000070.2(CAPN3):c.2362A>C (p.Arg788=) rs760891133
NM_000070.2(CAPN3):c.2380+12delA rs28364538
NM_000070.2(CAPN3):c.246G>A (p.Pro82=) rs146529432
NM_000070.2(CAPN3):c.270C>T (p.Ser90=) rs753686702
NM_000070.2(CAPN3):c.318C>T (p.Cys106=) rs117609395
NM_000070.2(CAPN3):c.319G>A (p.Glu107Lys) rs1801505
NM_000070.2(CAPN3):c.379+11G>A rs371195831
NM_000070.2(CAPN3):c.468C>T (p.Ile156=) rs143942248
NM_000070.2(CAPN3):c.479C>G (p.Ala160Gly) rs17592
NM_000070.2(CAPN3):c.495C>T (p.Phe165=) rs1801324
NM_000070.2(CAPN3):c.499-13C>T rs201344810
NM_000070.2(CAPN3):c.51C>T (p.Pro17=) rs1392565832
NM_000070.2(CAPN3):c.525C>T (p.Asp175=) rs144383442
NM_000070.2(CAPN3):c.551C>T (p.Thr184Met) rs35889956
NM_000070.2(CAPN3):c.552G>A (p.Thr184=) rs147808529
NM_000070.2(CAPN3):c.606T>C (p.Ser202=) rs17593
NM_000070.2(CAPN3):c.62G>A (p.Gly21Glu) rs28364364
NM_000070.2(CAPN3):c.78G>A (p.Pro26=) rs62642519
NM_000070.2(CAPN3):c.801+19G>A rs767858015
NM_000070.2(CAPN3):c.930T>C (p.Asp310=) rs150356488
NM_000070.2(CAPN3):c.939G>A (p.Pro313=) rs78369269
NM_000070.2(CAPN3):c.945+14C>T rs763112832
NM_000070.2(CAPN3):c.945+15G>A rs567256305
NM_000070.2(CAPN3):c.946-34G>A rs139297309
NM_000070.2(CAPN3):c.96T>C (p.Thr32=) rs1801496
NM_000070.2(CAPN3):c.984C>T (p.Cys328=) rs28364441

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