ClinVar Miner

List of variants in gene TXNRD2 reported as likely benign for Cardiovascular phenotype

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Total variants: 27
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HGVS dbSNP
NM_006440.5(TXNRD2):c.1016A>T (p.Gln339Leu) rs200606822
NM_006440.5(TXNRD2):c.1077C>T (p.Asp359=) rs147383232
NM_006440.5(TXNRD2):c.1137G>C (p.Val379=) rs184640901
NM_006440.5(TXNRD2):c.1174T>C (p.Tyr392His) rs201971987
NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=) rs544242322
NM_006440.5(TXNRD2):c.1195G>A (p.Val399Ile) rs201222740
NM_006440.5(TXNRD2):c.1308C>T (p.Phe436=) rs190301927
NM_006440.5(TXNRD2):c.1341T>G (p.Tyr447Ter) rs202059967
NM_006440.5(TXNRD2):c.1401C>T (p.Gly467=) rs886038873
NM_006440.5(TXNRD2):c.1407C>A (p.Asn469Lys) rs200063300
NM_006440.5(TXNRD2):c.1523G>A (p.Arg508His) rs201391000
NM_006440.5(TXNRD2):c.174C>T (p.Ala58=) rs767236339
NM_006440.5(TXNRD2):c.303A>G (p.Ala101=) rs200076623
NM_006440.5(TXNRD2):c.462C>T (p.Tyr154=) rs182857388
NM_006440.5(TXNRD2):c.505G>A (p.Gly169Ser) rs138462062
NM_006440.5(TXNRD2):c.64G>A (p.Val22Met) rs370819229
NM_006440.5(TXNRD2):c.650C>A (p.Ser217Tyr) rs201913959
NM_006440.5(TXNRD2):c.714C>T (p.Thr238=) rs202225486
NM_006440.5(TXNRD2):c.72C>A (p.Gly24=) rs1032624911
NM_006440.5(TXNRD2):c.762C>T (p.Arg254=) rs180876642
NM_006440.5(TXNRD2):c.816C>T (p.Gly272=) rs144584524
NM_006440.5(TXNRD2):c.846G>A (p.Ser282=) rs373979565
NM_006440.5(TXNRD2):c.858G>C (p.Arg286Ser) rs201503021
NM_006440.5(TXNRD2):c.903C>T (p.Thr301=) rs35695986
NM_006440.5(TXNRD2):c.917C>T (p.Thr306Met) rs371153395
NM_006440.5(TXNRD2):c.933C>T (p.Thr311=) rs187065627
NM_006440.5(TXNRD2):c.957C>G (p.Val319=) rs371700934

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