ClinVar Miner

List of variants in gene CAPN3 reported as likely benign by Invitae

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Gene type:
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Total variants: 21
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HGVS dbSNP
NM_000070.3(CAPN3):c.1020G>T (p.Gly340=) rs372401631
NM_000070.3(CAPN3):c.1227A>C (p.Thr409=) rs111806046
NM_000070.3(CAPN3):c.1227A>G (p.Thr409=) rs111806046
NM_000070.3(CAPN3):c.1263G>A (p.Leu421=) rs372450879
NM_000070.3(CAPN3):c.1410C>T (p.Asp470=) rs371148431
NM_000070.3(CAPN3):c.1584C>T (p.Asn528=) rs530529988
NM_000070.3(CAPN3):c.1668C>T (p.Ile556=) rs199884116
NM_000070.3(CAPN3):c.1746-7C>G rs199978708
NM_000070.3(CAPN3):c.1818G>A (p.Ser606=) rs28364528
NM_000070.3(CAPN3):c.183C>T (p.Phe61=) rs146069933
NM_000070.3(CAPN3):c.2088C>A (p.Ser696=) rs867628179
NM_000070.3(CAPN3):c.2109C>T (p.Leu703=) rs371577901
NM_000070.3(CAPN3):c.2154C>T (p.His718=) rs1351586112
NM_000070.3(CAPN3):c.2235C>T (p.Tyr745=) rs147774793
NM_000070.3(CAPN3):c.2292C>T (p.Asp764=) rs187279903
NM_000070.3(CAPN3):c.232C>A (p.Pro78Thr) rs138867099
NM_000070.3(CAPN3):c.2362A>C (p.Arg788=) rs760891133
NM_000070.3(CAPN3):c.270C>T (p.Ser90=) rs753686702
NM_000070.3(CAPN3):c.51C>T (p.Pro17=) rs1392565832
NM_000070.3(CAPN3):c.525C>T (p.Asp175=) rs144383442
NM_000070.3(CAPN3):c.552G>A (p.Thr184=) rs147808529

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