ClinVar Miner

List of variants in gene NEXN reported as likely benign for Dilated cardiomyopathy 1CC; Familial hypertrophic cardiomyopathy 20

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Total variants: 16
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HGVS dbSNP
NM_144573.3(NEXN):c.1029G>A (p.Ala343=) rs374260457
NM_144573.3(NEXN):c.1083T>C (p.Tyr361=) rs1060504549
NM_144573.3(NEXN):c.1089A>C (p.Thr363=) rs878855209
NM_144573.3(NEXN):c.1137A>G (p.Glu379=) rs1553240026
NM_144573.3(NEXN):c.1368A>C (p.Gly456=) rs397517845
NM_144573.3(NEXN):c.1582G>C (p.Glu528Gln) rs200071700
NM_144573.3(NEXN):c.1671_1673GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.3(NEXN):c.1743T>G (p.Ala581=) rs772313224
NM_144573.3(NEXN):c.222T>C (p.Ile74=) rs767610015
NM_144573.3(NEXN):c.237T>C (p.Ala79=) rs727504549
NM_144573.3(NEXN):c.299-10A>G rs1452768769
NM_144573.3(NEXN):c.321T>A (p.Ala107=) rs1553236762
NM_144573.3(NEXN):c.507A>G (p.Leu169=) rs776106290
NM_144573.3(NEXN):c.688-10G>A rs370574269
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.3(NEXN):c.949A>C (p.Met317Leu) rs559464457

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