ClinVar Miner

List of variants in gene TXNRD2 studied for not specified

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Gene type:
ClinVar version:
Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_006440.5(TXNRD2):c.1109T>C (p.Ile370Thr) rs1139793 0.77627
NM_006440.5(TXNRD2):c.177C>T (p.Ala59=) rs5748470 0.50192
NM_006440.5(TXNRD2):c.196G>T (p.Ala66Ser) rs5748469 0.35646
NM_006440.5(TXNRD2):c.1206G>A (p.Pro402=) rs1139795 0.27722
NM_006440.5(TXNRD2):c.774+14C>A rs12169091 0.25670
NM_006440.5(TXNRD2):c.1086+17G>A rs2239893 0.25106
NM_006440.5(TXNRD2):c.246C>T (p.Leu82=) rs11541479 0.20721
NM_006440.5(TXNRD2):c.662+14G>A rs9606176 0.13466
NM_006440.5(TXNRD2):c.1347+20A>G rs113605285 0.08271
NM_006440.5(TXNRD2):c.662+13C>T rs45550336 0.03292
NM_006440.5(TXNRD2):c.526G>C (p.Glu176Gln) rs61736929 0.02373
NM_006440.5(TXNRD2):c.374+13C>T rs9606178 0.02112
NM_006440.5(TXNRD2):c.1099C>T (p.Leu367=) rs35544159 0.01575
NM_006440.5(TXNRD2):c.1445+18C>T rs41431147 0.01166
NM_006440.5(TXNRD2):c.1233C>T (p.Ser411=) rs35099271 0.00966
NM_006440.5(TXNRD2):c.591+18del rs200848663 0.00807
NM_006440.5(TXNRD2):c.375-19T>G rs147120537 0.00527
NM_006440.5(TXNRD2):c.1087-11C>T rs577814757 0.00505
NM_006440.5(TXNRD2):c.816C>T (p.Gly272=) rs144584524 0.00266
NM_006440.5(TXNRD2):c.110A>T (p.Gln37Leu) rs148092370 0.00150
NM_006440.5(TXNRD2):c.374+17G>A rs200108545 0.00080
NM_006440.5(TXNRD2):c.592-17C>A rs375350567 0.00044
NM_006440.5(TXNRD2):c.662+11C>G rs373734411 0.00038
NM_006440.5(TXNRD2):c.229+15A>G rs370756162 0.00029
NM_006440.5(TXNRD2):c.1275+18C>T rs374333900 0.00023
NM_006440.5(TXNRD2):c.1086+12G>A rs143966577 0.00021
NM_006440.5(TXNRD2):c.173-19del rs770032943 0.00020
NM_006440.5(TXNRD2):c.1155G>C (p.Gly385=) rs370957634 0.00019
NM_006440.5(TXNRD2):c.1276-15G>A rs374202570 0.00014
NM_006440.5(TXNRD2):c.949+11G>A rs772807846 0.00007
NM_006440.5(TXNRD2):c.1176C>T (p.Tyr392=) rs544242322 0.00006
NM_006440.5(TXNRD2):c.1445+13G>T rs938029725 0.00006
NM_006440.5(TXNRD2):c.174C>T (p.Ala58=) rs767236339 0.00006
NM_006440.5(TXNRD2):c.528+19C>T rs746285839 0.00006
NM_006440.5(TXNRD2):c.1182+19C>T rs377040175 0.00004
NM_006440.5(TXNRD2):c.760C>T (p.Arg254Cys) rs183950022 0.00004
NM_006440.5(TXNRD2):c.1464G>A (p.Ala488=) rs372816982 0.00003
NM_006440.5(TXNRD2):c.1497A>G (p.Thr499=) rs969582646 0.00003
NM_006440.5(TXNRD2):c.449+17C>T rs370505160 0.00003
NM_006440.5(TXNRD2):c.489C>T (p.Asp163=) rs751116028 0.00003
NM_006440.5(TXNRD2):c.1086+11C>T rs369332144 0.00002
NM_006440.5(TXNRD2):c.1331C>G (p.Ser444Cys) rs749643976 0.00001
NM_006440.5(TXNRD2):c.172+20C>A rs760016716 0.00001
NM_006440.5(TXNRD2):c.588G>A (p.Thr196=) rs377699868 0.00001
NM_006440.5(TXNRD2):c.1107C>A (p.Pro369=) rs371533709
NM_006440.5(TXNRD2):c.1150G>A (p.Gly384Ser) rs192869629
NM_006440.5(TXNRD2):c.173-15T>C rs1555913241
NM_006440.5(TXNRD2):c.374+16C>A rs141500917
NM_006440.5(TXNRD2):c.450-15_450-14del rs767787404
NM_006440.5(TXNRD2):c.529-8C>T rs754998172
NM_006440.5(TXNRD2):c.592-20G>C rs1555911999
NM_006440.5(TXNRD2):c.592-5G>C rs1555911995
NM_006440.5(TXNRD2):c.682+16G>A rs377147143
NM_006440.5(TXNRD2):c.895A>C (p.Ser299Arg) rs5992495
NM_006440.5(TXNRD2):c.903C>A (p.Thr301=) rs35695986

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