ClinVar Miner

List of variants in gene TXNRD2 reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP gnomAD frequency
NM_006440.5(TXNRD2):c.816C>T (p.Gly272=) rs144584524 0.00266
NM_006440.5(TXNRD2):c.505G>A (p.Gly169Ser) rs138462062 0.00128
NM_006440.5(TXNRD2):c.933C>T (p.Thr311=) rs187065627 0.00108
NM_006440.5(TXNRD2):c.1016A>T (p.Gln339Leu) rs200606822 0.00106
NM_006440.5(TXNRD2):c.1195G>A (p.Val399Ile) rs201222740 0.00104
NM_006440.5(TXNRD2):c.1523G>A (p.Arg508His) rs201391000 0.00102
NM_006440.5(TXNRD2):c.762C>T (p.Arg254=) rs180876642 0.00101
NM_006440.5(TXNRD2):c.303A>G (p.Ala101=) rs200076623 0.00069
NM_006440.5(TXNRD2):c.858G>C (p.Arg286Ser) rs201503021 0.00064
NM_006440.5(TXNRD2):c.1461T>C (p.Tyr487=) rs376363162 0.00061
NM_006440.5(TXNRD2):c.1174T>C (p.Tyr392His) rs201971987 0.00052
NM_006440.5(TXNRD2):c.1509G>A (p.Glu503=) rs200619889 0.00045
NM_006440.5(TXNRD2):c.1499G>T (p.Cys500Phe) rs554063995 0.00044
NM_006440.5(TXNRD2):c.462C>T (p.Tyr154=) rs182857388 0.00038
NM_006440.5(TXNRD2):c.650C>A (p.Ser217Tyr) rs201913959 0.00036
NM_006440.5(TXNRD2):c.1308C>T (p.Phe436=) rs190301927 0.00031
NM_006440.5(TXNRD2):c.957C>G (p.Val319=) rs371700934 0.00024
NM_006440.5(TXNRD2):c.1077C>T (p.Asp359=) rs147383232 0.00021
NM_006440.5(TXNRD2):c.1137G>C (p.Val379=) rs184640901 0.00020
NM_006440.5(TXNRD2):c.1155G>C (p.Gly385=) rs370957634 0.00019
NM_006440.5(TXNRD2):c.585C>G (p.Pro195=) rs201760306 0.00019
NM_006440.5(TXNRD2):c.834C>G (p.Gly278=) rs371075332 0.00016
NM_006440.5(TXNRD2):c.1158C>T (p.Ser386=) rs558954630 0.00013
NM_006440.5(TXNRD2):c.1475G>A (p.Arg492Gln) rs368561764 0.00013
NM_006440.5(TXNRD2):c.821G>A (p.Arg274Gln) rs374364917 0.00013
NM_006440.5(TXNRD2):c.543C>T (p.Ala181=) rs367754522 0.00011
NM_006440.5(TXNRD2):c.801C>T (p.His267=) rs550803593 0.00010
NM_006440.5(TXNRD2):c.1224G>C (p.Val408=) rs375650172 0.00009
NM_006440.5(TXNRD2):c.135C>T (p.Val45=) rs752213778 0.00009
NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=) rs544242322 0.00006
NM_006440.5(TXNRD2):c.1341T>G (p.Tyr447Ter) rs202059967 0.00006
NM_006440.5(TXNRD2):c.174C>T (p.Ala58=) rs767236339 0.00006
NM_006440.5(TXNRD2):c.504C>T (p.Cys168=) rs752481782 0.00006
NM_006440.5(TXNRD2):c.714C>T (p.Thr238=) rs202225486 0.00006
NM_006440.5(TXNRD2):c.1008C>T (p.Pro336=) rs746370708 0.00005
NM_006440.5(TXNRD2):c.1413C>T (p.Gly471=) rs753841469 0.00005
NM_006440.5(TXNRD2):c.917C>T (p.Thr306Met) rs371153395 0.00005
NM_006440.5(TXNRD2):c.1149C>T (p.Phe383=) rs768999643 0.00004
NM_006440.5(TXNRD2):c.1305G>A (p.Glu435=) rs919971767 0.00004
NM_006440.5(TXNRD2):c.1368C>T (p.Pro456=) rs1388056453 0.00004
NM_006440.5(TXNRD2):c.760C>T (p.Arg254Cys) rs183950022 0.00004
NM_006440.5(TXNRD2):c.1497A>G (p.Thr499=) rs969582646 0.00003
NM_006440.5(TXNRD2):c.1554G>A (p.Thr518=) rs144497090 0.00003
NM_006440.5(TXNRD2):c.360C>T (p.Pro120=) rs780233789 0.00003
NM_006440.5(TXNRD2):c.489C>T (p.Asp163=) rs751116028 0.00003
NM_006440.5(TXNRD2):c.846G>A (p.Ser282=) rs373979565 0.00003
NM_006440.5(TXNRD2):c.1113G>A (p.Ala371=) rs745421312 0.00002
NM_006440.5(TXNRD2):c.1122C>T (p.Ala374=) rs780948248 0.00002
NM_006440.5(TXNRD2):c.1152C>T (p.Gly384=) rs766934707 0.00002
NM_006440.5(TXNRD2):c.1463C>T (p.Ala488Val) rs752947034 0.00002
NM_006440.5(TXNRD2):c.918G>A (p.Thr306=) rs763086193 0.00002
NM_006440.5(TXNRD2):c.1065C>T (p.Tyr355=) rs377072227 0.00001
NM_006440.5(TXNRD2):c.1131C>T (p.Leu377=) rs773930137 0.00001
NM_006440.5(TXNRD2):c.113G>A (p.Arg38Gln) rs777384922 0.00001
NM_006440.5(TXNRD2):c.1401C>T (p.Gly467=) rs886038873 0.00001
NM_006440.5(TXNRD2):c.1449T>C (p.Cys483=) rs1194743410 0.00001
NM_006440.5(TXNRD2):c.264C>T (p.Asn88=) rs575321083 0.00001
NM_006440.5(TXNRD2):c.366G>A (p.Pro122=) rs3747068 0.00001
NM_006440.5(TXNRD2):c.591C>T (p.His197=) rs543644944 0.00001
NM_006440.5(TXNRD2):c.845C>T (p.Ser282Leu) rs368200536 0.00001
NM_006440.5(TXNRD2):c.1002T>C (p.Thr334=) rs1938875775
NM_006440.5(TXNRD2):c.1011C>T (p.Asp337=)
NM_006440.5(TXNRD2):c.1107C>T (p.Pro369=)
NM_006440.5(TXNRD2):c.1122C>G (p.Ala374=)
NM_006440.5(TXNRD2):c.1125G>T (p.Gly375=)
NM_006440.5(TXNRD2):c.1161A>G (p.Ser387=)
NM_006440.5(TXNRD2):c.1191G>A (p.Thr397=) rs1292463748
NM_006440.5(TXNRD2):c.1200C>T (p.Phe400=)
NM_006440.5(TXNRD2):c.1257C>T (p.His419=)
NM_006440.5(TXNRD2):c.1311G>A (p.Thr437=)
NM_006440.5(TXNRD2):c.1387C>T (p.Leu463=)
NM_006440.5(TXNRD2):c.138C>T (p.Gly46=)
NM_006440.5(TXNRD2):c.1407C>A (p.Asn469Lys) rs200063300
NM_006440.5(TXNRD2):c.1500C>T (p.Cys500=)
NM_006440.5(TXNRD2):c.1515C>T (p.Val505=)
NM_006440.5(TXNRD2):c.198C>T (p.Ala66=)
NM_006440.5(TXNRD2):c.249C>T (p.Gly83=)
NM_006440.5(TXNRD2):c.258C>T (p.Cys86=)
NM_006440.5(TXNRD2):c.300G>A (p.Ala100=)
NM_006440.5(TXNRD2):c.307C>T (p.Leu103=)
NM_006440.5(TXNRD2):c.312A>C (p.Gly104=)
NM_006440.5(TXNRD2):c.408G>A (p.Val136=)
NM_006440.5(TXNRD2):c.426C>T (p.Gly142=)
NM_006440.5(TXNRD2):c.42C>T (p.Arg14=)
NM_006440.5(TXNRD2):c.471C>A (p.Ile157=)
NM_006440.5(TXNRD2):c.486T>C (p.Val162=)
NM_006440.5(TXNRD2):c.486T>G (p.Val162=)
NM_006440.5(TXNRD2):c.534G>T (p.Leu178=)
NM_006440.5(TXNRD2):c.724C>T (p.Leu242=)
NM_006440.5(TXNRD2):c.762C>A (p.Arg254=)
NM_006440.5(TXNRD2):c.768C>T (p.Phe256=)
NM_006440.5(TXNRD2):c.822G>A (p.Arg274=)
NM_006440.5(TXNRD2):c.855G>A (p.Arg285=)
NM_006440.5(TXNRD2):c.858G>A (p.Arg286=) rs201503021
NM_006440.5(TXNRD2):c.903C>T (p.Thr301=) rs35695986
NM_006440.5(TXNRD2):c.933C>A (p.Thr311=)
NM_006440.5(TXNRD2):c.987G>A (p.Lys329=) rs1454322676

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