ClinVar Miner

List of variants in gene TXNRD2 reported as benign

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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP
NM_006440.5(TXNRD2):c.103+340G>A
NM_006440.5(TXNRD2):c.103+81dup rs45511293
NM_006440.5(TXNRD2):c.1077C>T (p.Asp359=) rs147383232
NM_006440.5(TXNRD2):c.1086+17G>A rs2239893
NM_006440.5(TXNRD2):c.1087-11C>T rs577814757
NM_006440.5(TXNRD2):c.1087-16del rs34827823
NM_006440.5(TXNRD2):c.1099C>T (p.Leu367=) rs35544159
NM_006440.5(TXNRD2):c.1109T>C (p.Ile370Thr) rs1139793
NM_006440.5(TXNRD2):c.110A>T (p.Gln37Leu) rs148092370
NM_006440.5(TXNRD2):c.1137G>C (p.Val379=) rs184640901
NM_006440.5(TXNRD2):c.1150G>A (p.Gly384Ser) rs192869629
NM_006440.5(TXNRD2):c.1158C>T (p.Ser386=) rs558954630
NM_006440.5(TXNRD2):c.1206G>A (p.Pro402=) rs1139795
NM_006440.5(TXNRD2):c.1233C>T (p.Ser411=) rs35099271
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.1347+20A>G rs113605285
NM_006440.5(TXNRD2):c.1445+18C>T rs41431147
NM_006440.5(TXNRD2):c.1445+254G>A rs16984300
NM_006440.5(TXNRD2):c.1446-203G>A rs73381892
NM_006440.5(TXNRD2):c.1461T>C (p.Tyr487=) rs376363162
NM_006440.5(TXNRD2):c.1509G>A (p.Glu503=) rs200619889
NM_006440.5(TXNRD2):c.173-224A>G rs17745433
NM_006440.5(TXNRD2):c.173-70T>C rs5748471
NM_006440.5(TXNRD2):c.177C>T (p.Ala59=) rs5748470
NM_006440.5(TXNRD2):c.196G>T (p.Ala66Ser) rs5748469
NM_006440.5(TXNRD2):c.210C>T (p.Tyr70=) rs186462665
NM_006440.5(TXNRD2):c.230-168_230-167del rs146802029
NM_006440.5(TXNRD2):c.246C>T (p.Leu82=) rs11541479
NM_006440.5(TXNRD2):c.374+127C>T rs34751052
NM_006440.5(TXNRD2):c.374+13C>T rs9606178
NM_006440.5(TXNRD2):c.374+16C>A rs141500917
NM_006440.5(TXNRD2):c.374+287G>A rs5993865
NM_006440.5(TXNRD2):c.374+77G>C rs3747067
NM_006440.5(TXNRD2):c.375-128C>A rs34776119
NM_006440.5(TXNRD2):c.375-62C>T rs756661
NM_006440.5(TXNRD2):c.449+111G>A rs77573782
NM_006440.5(TXNRD2):c.450-292C>T rs115268335
NM_006440.5(TXNRD2):c.462C>T (p.Tyr154=) rs182857388
NM_006440.5(TXNRD2):c.526G>C (p.Glu176Gln) rs61736929
NM_006440.5(TXNRD2):c.529-118C>G rs114905700
NM_006440.5(TXNRD2):c.529-6C>T rs116054286
NM_006440.5(TXNRD2):c.529-97G>A rs2073771
NM_006440.5(TXNRD2):c.591+18del rs200848663
NM_006440.5(TXNRD2):c.591+211A>G rs4597638
NM_006440.5(TXNRD2):c.591+66G>A rs16982755
NM_006440.5(TXNRD2):c.662+13C>T rs45550336
NM_006440.5(TXNRD2):c.662+14G>A rs9606176
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.683-6C>T rs757160421
NM_006440.5(TXNRD2):c.68C>A (p.Ala23Glu) rs532340383
NM_006440.5(TXNRD2):c.763G>C (p.Gly255Arg) rs76079250
NM_006440.5(TXNRD2):c.774+14C>A rs12169091
NM_006440.5(TXNRD2):c.775-85T>C rs78239309
NM_006440.5(TXNRD2):c.816C>T (p.Gly272=) rs144584524
NM_006440.5(TXNRD2):c.895A>C (p.Ser299Arg) rs5992495
NM_006440.5(TXNRD2):c.903C>A (p.Thr301=) rs35695986
NM_006440.5(TXNRD2):c.933C>T (p.Thr311=) rs187065627
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

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