ClinVar Miner

List of variants in gene TXNRD2 studied for not provided

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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP
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.103+278C>T rs45559342
NM_006440.5(TXNRD2):c.103+81dup rs45511293
NM_006440.5(TXNRD2):c.104-102C>T rs79960807
NM_006440.5(TXNRD2):c.1087-8T>C rs1000041198
NM_006440.5(TXNRD2):c.1104A>G (p.Thr368=) rs1601384637
NM_006440.5(TXNRD2):c.1122C>T (p.Ala374=) rs780948248
NM_006440.5(TXNRD2):c.1158C>T (p.Ser386=) rs558954630
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.1182+49C>T rs73381902
NM_006440.5(TXNRD2):c.1211A>G (p.Glu404Gly) rs1435686741
NM_006440.5(TXNRD2):c.1275+163G>C rs11913319
NM_006440.5(TXNRD2):c.1275+198T>C rs76576226
NM_006440.5(TXNRD2):c.1276-234C>G rs5993849
NM_006440.5(TXNRD2):c.1322G>A (p.Arg441Gln) rs759374389
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.1445+254G>A rs16984300
NM_006440.5(TXNRD2):c.1446-203G>A rs73381892
NM_006440.5(TXNRD2):c.1446-70C>T rs116583868
NM_006440.5(TXNRD2):c.1464G>A (p.Ala488=) rs372816982
NM_006440.5(TXNRD2):c.1479C>T (p.Thr493=) rs767844402
NM_006440.5(TXNRD2):c.1484G>A (p.Gly495Asp) rs773949487
NM_006440.5(TXNRD2):c.172+182C>T rs114490696
NM_006440.5(TXNRD2):c.173-224A>G rs17745433
NM_006440.5(TXNRD2):c.173-70T>C rs5748471
NM_006440.5(TXNRD2):c.230-168_230-167del rs146802029
NM_006440.5(TXNRD2):c.259G>A (p.Val87Ile) rs201658653
NM_006440.5(TXNRD2):c.264C>T (p.Asn88=) rs575321083
NM_006440.5(TXNRD2):c.374+127C>T rs34751052
NM_006440.5(TXNRD2):c.374+287G>A rs5993865
NM_006440.5(TXNRD2):c.374+77G>C rs3747067
NM_006440.5(TXNRD2):c.374+87C>A rs138368791
NM_006440.5(TXNRD2):c.375-128C>A rs34776119
NM_006440.5(TXNRD2):c.375-62C>T rs756661
NM_006440.5(TXNRD2):c.40C>T (p.Arg14Cys) rs1259706318
NM_006440.5(TXNRD2):c.417del (p.Asn140fs) rs780054798
NM_006440.5(TXNRD2):c.449+111G>A rs77573782
NM_006440.5(TXNRD2):c.450-292C>T rs115268335
NM_006440.5(TXNRD2):c.450-75G>C rs79661740
NM_006440.5(TXNRD2):c.497C>T (p.Thr166Met) rs553337931
NM_006440.5(TXNRD2):c.529-118C>G rs114905700
NM_006440.5(TXNRD2):c.529-97G>A rs2073771
NM_006440.5(TXNRD2):c.591+211A>G rs4597638
NM_006440.5(TXNRD2):c.591+243C>G rs145232439
NM_006440.5(TXNRD2):c.591+66G>A rs16982755
NM_006440.5(TXNRD2):c.63C>T (p.Ala21=) rs562298402
NM_006440.5(TXNRD2):c.662+240del rs149796774
NM_006440.5(TXNRD2):c.662+63T>C rs885987
NM_006440.5(TXNRD2):c.663-206C>T rs8142006
NM_006440.5(TXNRD2):c.682+15C>T rs201450101
NM_006440.5(TXNRD2):c.683-6C>T rs757160421
NM_006440.5(TXNRD2):c.68C>A (p.Ala23Glu) rs532340383
NM_006440.5(TXNRD2):c.714C>T (p.Thr238=) rs202225486
NM_006440.5(TXNRD2):c.715G>A (p.Gly239Arg) rs978493213
NM_006440.5(TXNRD2):c.745C>T (p.Arg249Cys) rs557142042
NM_006440.5(TXNRD2):c.756C>T (p.Pro252=) rs1371426999
NM_006440.5(TXNRD2):c.774+255C>A rs144567421
NM_006440.5(TXNRD2):c.775-85T>C rs78239309
NM_006440.5(TXNRD2):c.849G>T (p.Arg283=) rs559964753
NM_006440.5(TXNRD2):c.868G>A (p.Gly290Ser) rs777357363
NM_006440.5(TXNRD2):c.903C>T (p.Thr301=) rs35695986
NM_006440.5(TXNRD2):c.904G>A (p.Gly302Ser) rs781228620
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.949+222C>T
NM_006440.5(TXNRD2):c.949+300C>T rs5993856
NM_006440.5(TXNRD2):c.949+42C>T rs5992494
NM_006440.5(TXNRD2):c.950-113G>C rs13057374
NM_006440.5(TXNRD2):c.950-214G>A rs114054391
NM_006440.5(TXNRD2):c.950-220A>G rs5992492
NM_006440.5(TXNRD2):c.950-80C>G rs145029690
NM_006440.5(TXNRD2):c.987G>A (p.Lys329=) rs1454322676

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