ClinVar Miner

List of variants in gene TXNRD2 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP
NM_006440.5(TXNRD2):c.1008C>T (p.Pro336=)
NM_006440.5(TXNRD2):c.1016A>T (p.Gln339Leu) rs200606822
NM_006440.5(TXNRD2):c.1029G>A (p.Val343=) rs758006460
NM_006440.5(TXNRD2):c.1032C>T (p.Asp344=)
NM_006440.5(TXNRD2):c.1087-8T>C rs1000041198
NM_006440.5(TXNRD2):c.1104A>G (p.Thr368=) rs1601384637
NM_006440.5(TXNRD2):c.1113G>A (p.Ala371=)
NM_006440.5(TXNRD2):c.1122C>T (p.Ala374=) rs780948248
NM_006440.5(TXNRD2):c.1131C>T (p.Leu377=)
NM_006440.5(TXNRD2):c.1149C>T (p.Phe383=) rs768999643
NM_006440.5(TXNRD2):c.1155G>C (p.Gly385=) rs370957634
NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=) rs544242322
NM_006440.5(TXNRD2):c.1194C>T (p.Thr398=) rs372301925
NM_006440.5(TXNRD2):c.1195G>A (p.Val399Ile) rs201222740
NM_006440.5(TXNRD2):c.1276-6C>T
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.135C>T (p.Val45=) rs752213778
NM_006440.5(TXNRD2):c.1375C>T (p.Leu459=)
NM_006440.5(TXNRD2):c.1381C>T (p.Leu461=)
NM_006440.5(TXNRD2):c.1383G>A (p.Leu461=)
NM_006440.5(TXNRD2):c.1398T>C (p.Leu466=) rs781691483
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.1407C>T (p.Asn469=)
NM_006440.5(TXNRD2):c.1422T>G (p.Thr474=)
NM_006440.5(TXNRD2):c.1445+9C>T
NM_006440.5(TXNRD2):c.1464G>A (p.Ala488=) rs372816982
NM_006440.5(TXNRD2):c.1474C>T (p.Arg492Trp)
NM_006440.5(TXNRD2):c.1479C>T (p.Thr493=) rs767844402
NM_006440.5(TXNRD2):c.1499G>T (p.Cys500Phe)
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.230-8C>T
NM_006440.5(TXNRD2):c.230-9A>G
NM_006440.5(TXNRD2):c.264C>T (p.Asn88=) rs575321083
NM_006440.5(TXNRD2):c.303A>G (p.Ala101=) rs200076623
NM_006440.5(TXNRD2):c.360C>T (p.Pro120=)
NM_006440.5(TXNRD2):c.366G>A (p.Pro122=)
NM_006440.5(TXNRD2):c.375-8C>T rs180876844
NM_006440.5(TXNRD2):c.489C>T (p.Asp163=) rs751116028
NM_006440.5(TXNRD2):c.504C>T (p.Cys168=) rs752481782
NM_006440.5(TXNRD2):c.505G>A (p.Gly169Ser) rs138462062
NM_006440.5(TXNRD2):c.507C>T (p.Gly169=)
NM_006440.5(TXNRD2):c.529-5C>T rs766288973
NM_006440.5(TXNRD2):c.543C>T (p.Ala181=) rs367754522
NM_006440.5(TXNRD2):c.585C>G (p.Pro195=) rs201760306
NM_006440.5(TXNRD2):c.588G>A (p.Thr196=) rs377699868
NM_006440.5(TXNRD2):c.63C>T (p.Ala21=) rs562298402
NM_006440.5(TXNRD2):c.650C>A (p.Ser217Tyr) rs201913959
NM_006440.5(TXNRD2):c.662+10G>T
NM_006440.5(TXNRD2):c.662+9T>G
NM_006440.5(TXNRD2):c.672C>T (p.Val224=)
NM_006440.5(TXNRD2):c.714C>T (p.Thr238=) rs202225486
NM_006440.5(TXNRD2):c.756C>T (p.Pro252=) rs1371426999
NM_006440.5(TXNRD2):c.762C>T (p.Arg254=) rs180876642
NM_006440.5(TXNRD2):c.801C>T (p.His267=)
NM_006440.5(TXNRD2):c.834C>A (p.Gly278=)
NM_006440.5(TXNRD2):c.849G>T (p.Arg283=) rs559964753
NM_006440.5(TXNRD2):c.858G>A (p.Arg286=) rs201503021
NM_006440.5(TXNRD2):c.858G>C (p.Arg286Ser) rs201503021
NM_006440.5(TXNRD2):c.861C>T (p.Leu287=)
NM_006440.5(TXNRD2):c.903C>T (p.Thr301=) rs35695986
NM_006440.5(TXNRD2):c.912G>A (p.Glu304=) rs751531927
NM_006440.5(TXNRD2):c.939G>A (p.Leu313=) rs1060504228
NM_006440.5(TXNRD2):c.949+10C>T rs563775080
NM_006440.5(TXNRD2):c.957C>G (p.Val319=) rs371700934
NM_006440.5(TXNRD2):c.96C>T (p.Gly32=) rs767140410
NM_006440.5(TXNRD2):c.987G>A (p.Lys329=) rs1454322676

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