ClinVar Miner

List of variants in gene TXNRD2 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
Download table as spreadsheet
HGVS dbSNP
NM_006440.5(TXNRD2):c.103+14dup rs756452923
NM_006440.5(TXNRD2):c.103+19G>A rs45536341
NM_006440.5(TXNRD2):c.1077C>T (p.Asp359=) rs147383232
NM_006440.5(TXNRD2):c.1086+11C>T rs369332144
NM_006440.5(TXNRD2):c.1086+12G>A rs143966577
NM_006440.5(TXNRD2):c.1107C>A (p.Pro369=) rs371533709
NM_006440.5(TXNRD2):c.1122C>T (p.Ala374=) rs780948248
NM_006440.5(TXNRD2):c.1137G>C (p.Val379=) rs184640901
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.1177G>A (p.Asp393Asn) rs369142382
NM_006440.5(TXNRD2):c.1182+19C>T rs377040175
NM_006440.5(TXNRD2):c.1182+20G>A rs369759249
NM_006440.5(TXNRD2):c.1275+18C>T rs374333900
NM_006440.5(TXNRD2):c.1276-15G>A rs374202570
NM_006440.5(TXNRD2):c.1308C>T (p.Phe436=) rs190301927
NM_006440.5(TXNRD2):c.135C>T (p.Val45=) rs752213778
NM_006440.5(TXNRD2):c.1445+13G>T rs938029725
NM_006440.5(TXNRD2):c.1464G>A (p.Ala488=) rs372816982
NM_006440.5(TXNRD2):c.1497A>G (p.Thr499=) rs969582646
NM_006440.5(TXNRD2):c.1509G>A (p.Glu503=) rs200619889
NM_006440.5(TXNRD2):c.1523G>A (p.Arg508His) rs201391000
NM_006440.5(TXNRD2):c.172+20C>A rs760016716
NM_006440.5(TXNRD2):c.173-15T>C rs1555913241
NM_006440.5(TXNRD2):c.173-19del rs770032943
NM_006440.5(TXNRD2):c.174C>T (p.Ala58=) rs767236339
NM_006440.5(TXNRD2):c.229+15A>G rs370756162
NM_006440.5(TXNRD2):c.303A>G (p.Ala101=) rs200076623
NM_006440.5(TXNRD2):c.374+17G>A rs200108545
NM_006440.5(TXNRD2):c.375-19T>G rs147120537
NM_006440.5(TXNRD2):c.375-8C>T rs180876844
NM_006440.5(TXNRD2):c.449+17C>T rs370505160
NM_006440.5(TXNRD2):c.449+4C>T rs755751835
NM_006440.5(TXNRD2):c.450-15_450-14del rs767787404
NM_006440.5(TXNRD2):c.462C>T (p.Tyr154=) rs182857388
NM_006440.5(TXNRD2):c.489C>T (p.Asp163=) rs751116028
NM_006440.5(TXNRD2):c.505G>A (p.Gly169Ser) rs138462062
NM_006440.5(TXNRD2):c.528+19C>T rs746285839
NM_006440.5(TXNRD2):c.529-6C>T rs116054286
NM_006440.5(TXNRD2):c.529-8C>T rs754998172
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.592-17C>A rs375350567
NM_006440.5(TXNRD2):c.592-20G>C rs1555911999
NM_006440.5(TXNRD2):c.592-5G>C rs1555911995
NM_006440.5(TXNRD2):c.63C>T (p.Ala21=) rs562298402
NM_006440.5(TXNRD2):c.64G>A (p.Val22Met) rs370819229
NM_006440.5(TXNRD2):c.662+11C>G rs373734411
NM_006440.5(TXNRD2):c.682+16G>A rs377147143
NM_006440.5(TXNRD2):c.683-6C>T rs757160421
NM_006440.5(TXNRD2):c.68C>A (p.Ala23Glu) rs532340383
NM_006440.5(TXNRD2):c.762C>T (p.Arg254=) rs180876642
NM_006440.5(TXNRD2):c.763G>C (p.Gly255Arg) rs76079250
NM_006440.5(TXNRD2):c.775-19G>A rs189646218
NM_006440.5(TXNRD2):c.816C>T (p.Gly272=) rs144584524
NM_006440.5(TXNRD2):c.933C>T (p.Thr311=) rs187065627
NM_006440.5(TXNRD2):c.949+11G>A rs772807846
NM_006440.5(TXNRD2):c.957C>G (p.Val319=) rs371700934

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.