ClinVar Miner

List of variants in gene TXNRD2 reported as uncertain significance by Invitae

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Gene type:
ClinVar version:
Total variants: 127
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HGVS dbSNP
NC_000022.11:g.(?_19911357)_(19911467_?)del
NC_000022.11:g.(?_19911367)_(19911457_?)del
NM_006440.5(TXNRD2):c.1011C>A (p.Asp337Glu) rs1569073275
NM_006440.5(TXNRD2):c.1030G>T (p.Asp344Tyr) rs373839226
NM_006440.5(TXNRD2):c.1037G>A (p.Arg346Gln) rs201349663
NM_006440.5(TXNRD2):c.104-1G>A
NM_006440.5(TXNRD2):c.104-3C>G
NM_006440.5(TXNRD2):c.1054C>A (p.Pro352Thr) rs1388529732
NM_006440.5(TXNRD2):c.1058A>C (p.His353Pro)
NM_006440.5(TXNRD2):c.1078G>A (p.Val360Met)
NM_006440.5(TXNRD2):c.1087-2A>G
NM_006440.5(TXNRD2):c.1091G>A (p.Arg364Gln) rs199734322
NM_006440.5(TXNRD2):c.1118T>C (p.Met373Thr)
NM_006440.5(TXNRD2):c.1123G>A (p.Gly375Arg)
NM_006440.5(TXNRD2):c.1123G>C (p.Gly375Arg)
NM_006440.5(TXNRD2):c.1126A>G (p.Arg376Gly)
NM_006440.5(TXNRD2):c.112C>T (p.Arg38Trp)
NM_006440.5(TXNRD2):c.113G>A (p.Arg38Gln) rs777384922
NM_006440.5(TXNRD2):c.1142G>A (p.Arg381Gln) rs774909194
NM_006440.5(TXNRD2):c.1150G>C (p.Gly384Arg)
NM_006440.5(TXNRD2):c.1152C>T (p.Gly384=)
NM_006440.5(TXNRD2):c.1153G>A (p.Gly385Arg)
NM_006440.5(TXNRD2):c.1154G>C (p.Gly385Ala)
NM_006440.5(TXNRD2):c.1156T>C (p.Ser386Pro)
NM_006440.5(TXNRD2):c.1157C>A (p.Ser386Tyr)
NM_006440.5(TXNRD2):c.1174T>C (p.Tyr392His) rs201971987
NM_006440.5(TXNRD2):c.1182T>C (p.Asn394=)
NM_006440.5(TXNRD2):c.1183-10_1183-7del rs1569070709
NM_006440.5(TXNRD2):c.1234G>A (p.Glu412Lys) rs781432469
NM_006440.5(TXNRD2):c.1266G>C (p.Glu422Asp) rs1569070557
NM_006440.5(TXNRD2):c.1280A>G (p.Tyr427Cys)
NM_006440.5(TXNRD2):c.1285G>A (p.Ala429Thr)
NM_006440.5(TXNRD2):c.1289A>C (p.His430Pro) rs376463546
NM_006440.5(TXNRD2):c.1321C>T (p.Arg441Ter) rs200162480
NM_006440.5(TXNRD2):c.1334A>G (p.Gln445Arg)
NM_006440.5(TXNRD2):c.1348-2A>G
NM_006440.5(TXNRD2):c.1370dup (p.Gln458fs)
NM_006440.5(TXNRD2):c.1376T>C (p.Leu459Pro)
NM_006440.5(TXNRD2):c.1378G>A (p.Val460Met)
NM_006440.5(TXNRD2):c.139G>A (p.Gly47Arg)
NM_006440.5(TXNRD2):c.1406A>G (p.Asn469Ser) rs757704344
NM_006440.5(TXNRD2):c.1407C>G (p.Asn469Lys) rs200063300
NM_006440.5(TXNRD2):c.1412G>A (p.Gly471Asp) rs754916024
NM_006440.5(TXNRD2):c.1414G>A (p.Glu472Lys) rs766076027
NM_006440.5(TXNRD2):c.1436T>C (p.Leu479Pro) rs756559860
NM_006440.5(TXNRD2):c.1445A>C (p.Lys482Thr)
NM_006440.5(TXNRD2):c.1451G>A (p.Gly484Glu)
NM_006440.5(TXNRD2):c.1453G>T (p.Ala485Ser) rs960962542
NM_006440.5(TXNRD2):c.1463C>T (p.Ala488Val)
NM_006440.5(TXNRD2):c.1465C>T (p.Gln489Ter) rs759650391
NM_006440.5(TXNRD2):c.1475G>A (p.Arg492Gln)
NM_006440.5(TXNRD2):c.1480G>A (p.Val494Met)
NM_006440.5(TXNRD2):c.1492C>T (p.Pro498Ser)
NM_006440.5(TXNRD2):c.1534C>T (p.Arg512Cys)
NM_006440.5(TXNRD2):c.1535G>A (p.Arg512His)
NM_006440.5(TXNRD2):c.1559C>G (p.Thr520Arg)
NM_006440.5(TXNRD2):c.172+3A>G rs923193498
NM_006440.5(TXNRD2):c.172G>A (p.Ala58Thr) rs764378793
NM_006440.5(TXNRD2):c.177_178delinsTT (p.Gln60Ter)
NM_006440.5(TXNRD2):c.199G>A (p.Val67Met) rs372803804
NM_006440.5(TXNRD2):c.205G>T (p.Asp69Tyr)
NM_006440.5(TXNRD2):c.214G>A (p.Glu72Lys) rs779740988
NM_006440.5(TXNRD2):c.221C>G (p.Ser74Cys) rs200942544
NM_006440.5(TXNRD2):c.224C>T (p.Pro75Leu)
NM_006440.5(TXNRD2):c.236G>A (p.Arg79Gln) rs373979810
NM_006440.5(TXNRD2):c.238T>C (p.Trp80Arg) rs762714876
NM_006440.5(TXNRD2):c.259G>A (p.Val87Ile) rs201658653
NM_006440.5(TXNRD2):c.299C>A (p.Ala100Glu)
NM_006440.5(TXNRD2):c.338A>G (p.Tyr113Cys) rs905391308
NM_006440.5(TXNRD2):c.361G>A (p.Val121Met)
NM_006440.5(TXNRD2):c.364C>T (p.Pro122Ser)
NM_006440.5(TXNRD2):c.375-7T>G rs1060501405
NM_006440.5(TXNRD2):c.380A>G (p.Lys127Arg) rs753524446
NM_006440.5(TXNRD2):c.382A>T (p.Met128Leu)
NM_006440.5(TXNRD2):c.392C>G (p.Ala131Gly)
NM_006440.5(TXNRD2):c.403del (p.His135fs)
NM_006440.5(TXNRD2):c.406G>A (p.Val136Met)
NM_006440.5(TXNRD2):c.417del (p.Asn140fs) rs780054798
NM_006440.5(TXNRD2):c.41_42delinsTT (p.Arg14Leu)
NM_006440.5(TXNRD2):c.431G>A (p.Arg144His) rs748674090
NM_006440.5(TXNRD2):c.449+10C>G
NM_006440.5(TXNRD2):c.449+3A>G
NM_006440.5(TXNRD2):c.449G>A (p.Arg150Lys)
NM_006440.5(TXNRD2):c.450-1G>A
NM_006440.5(TXNRD2):c.461A>T (p.Tyr154Phe)
NM_006440.5(TXNRD2):c.479G>A (p.Ser160Asn)
NM_006440.5(TXNRD2):c.52C>T (p.Arg18Trp) rs1060501404
NM_006440.5(TXNRD2):c.571C>T (p.Arg191Trp)
NM_006440.5(TXNRD2):c.587C>T (p.Thr196Met)
NM_006440.5(TXNRD2):c.589C>G (p.His197Asp) rs762695606
NM_006440.5(TXNRD2):c.591+1G>A
NM_006440.5(TXNRD2):c.591+1G>C rs200610775
NM_006440.5(TXNRD2):c.595G>A (p.Glu199Lys)
NM_006440.5(TXNRD2):c.599G>A (p.Gly200Asp)
NM_006440.5(TXNRD2):c.611A>G (p.Tyr204Cys) rs199765650
NM_006440.5(TXNRD2):c.623G>A (p.Ser208Asn)
NM_006440.5(TXNRD2):c.64G>A (p.Val22Met) rs370819229
NM_006440.5(TXNRD2):c.64G>T (p.Val22Leu) rs370819229
NM_006440.5(TXNRD2):c.655G>C (p.Gly219Arg)
NM_006440.5(TXNRD2):c.656G>C (p.Gly219Ala) rs199510610
NM_006440.5(TXNRD2):c.662+1G>A rs1317400468
NM_006440.5(TXNRD2):c.662+6G>A rs887858049
NM_006440.5(TXNRD2):c.662C>T (p.Thr221Met)
NM_006440.5(TXNRD2):c.704G>C (p.Gly235Ala) rs1259831281
NM_006440.5(TXNRD2):c.720T>G (p.Ile240Met)
NM_006440.5(TXNRD2):c.745C>T (p.Arg249Cys) rs557142042
NM_006440.5(TXNRD2):c.746G>A (p.Arg249His) rs760799626
NM_006440.5(TXNRD2):c.775C>A (p.Gln259Lys)
NM_006440.5(TXNRD2):c.77T>G (p.Val26Gly) rs925920723
NM_006440.5(TXNRD2):c.77_83dup (p.Ala30fs)
NM_006440.5(TXNRD2):c.789G>A (p.Met263Ile)
NM_006440.5(TXNRD2):c.821G>A (p.Arg274Gln) rs374364917
NM_006440.5(TXNRD2):c.834C>G (p.Gly278=) rs371075332
NM_006440.5(TXNRD2):c.845C>T (p.Ser282Leu) rs368200536
NM_006440.5(TXNRD2):c.847C>T (p.Arg283Trp)
NM_006440.5(TXNRD2):c.850G>C (p.Val284Leu) rs201177571
NM_006440.5(TXNRD2):c.860T>G (p.Leu287Arg) rs989125451
NM_006440.5(TXNRD2):c.868G>A (p.Gly290Ser) rs777357363
NM_006440.5(TXNRD2):c.869G>T (p.Gly290Val) rs543290126
NM_006440.5(TXNRD2):c.88G>T (p.Ala30Ser) rs1315091228
NM_006440.5(TXNRD2):c.904G>A (p.Gly302Ser) rs781228620
NM_006440.5(TXNRD2):c.90_101dup (p.27_30RGAA[3]) rs1008629337
NM_006440.5(TXNRD2):c.917C>T (p.Thr306Met) rs371153395
NM_006440.5(TXNRD2):c.958C>T (p.Pro320Ser)
NM_006440.5(TXNRD2):c.965C>A (p.Thr322Asn)
NM_006440.5(TXNRD2):c.965C>G (p.Thr322Ser)
NM_006440.5(TXNRD2):c.974T>C (p.Leu325Pro) rs759476139

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