ClinVar Miner

List of variants in gene TXNRD2 reported as benign for Primary dilated cardiomyopathy

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Total variants: 25
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HGVS dbSNP
NM_006440.5(TXNRD2):c.103+340G>A
NM_006440.5(TXNRD2):c.1077C>T (p.Asp359=) rs147383232
NM_006440.5(TXNRD2):c.1099C>T (p.Leu367=) rs35544159
NM_006440.5(TXNRD2):c.1109T>C (p.Ile370Thr) rs1139793
NM_006440.5(TXNRD2):c.110A>T (p.Gln37Leu) rs148092370
NM_006440.5(TXNRD2):c.1137G>C (p.Val379=) rs184640901
NM_006440.5(TXNRD2):c.1150G>A (p.Gly384Ser) rs192869629
NM_006440.5(TXNRD2):c.1206G>A (p.Pro402=) rs1139795
NM_006440.5(TXNRD2):c.1233C>T (p.Ser411=) rs35099271
NM_006440.5(TXNRD2):c.1461T>C (p.Tyr487=) rs376363162
NM_006440.5(TXNRD2):c.1509G>A (p.Glu503=) rs200619889
NM_006440.5(TXNRD2):c.177C>T (p.Ala59=) rs5748470
NM_006440.5(TXNRD2):c.196G>T (p.Ala66Ser) rs5748469
NM_006440.5(TXNRD2):c.210C>T (p.Tyr70=) rs186462665
NM_006440.5(TXNRD2):c.246C>T (p.Leu82=) rs11541479
NM_006440.5(TXNRD2):c.462C>T (p.Tyr154=) rs182857388
NM_006440.5(TXNRD2):c.526G>C (p.Glu176Gln) rs61736929
NM_006440.5(TXNRD2):c.529-6C>T rs116054286
NM_006440.5(TXNRD2):c.683-6C>T rs757160421
NM_006440.5(TXNRD2):c.68C>A (p.Ala23Glu) rs532340383
NM_006440.5(TXNRD2):c.763G>C (p.Gly255Arg) rs76079250
NM_006440.5(TXNRD2):c.816C>T (p.Gly272=) rs144584524
NM_006440.5(TXNRD2):c.895A>C (p.Ser299Arg) rs5992495
NM_006440.5(TXNRD2):c.903C>A (p.Thr301=) rs35695986
NM_006440.5(TXNRD2):c.933C>T (p.Thr311=) rs187065627

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