ClinVar Miner

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

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Gene type:
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Total variants: 23
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HGVS dbSNP
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.1150G>A (p.Gly384Ser) rs192869629
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.1347+20A>G rs113605285
NM_006440.5(TXNRD2):c.1445+18C>T rs41431147
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.246C>T (p.Leu82=) rs11541479
NM_006440.5(TXNRD2):c.374+13C>T rs9606178
NM_006440.5(TXNRD2):c.374+16C>A rs141500917
NM_006440.5(TXNRD2):c.526G>C (p.Glu176Gln) rs61736929
NM_006440.5(TXNRD2):c.591+18del rs200848663
NM_006440.5(TXNRD2):c.662+13C>T rs45550336
NM_006440.5(TXNRD2):c.662+14G>A rs9606176
NM_006440.5(TXNRD2):c.774+14C>A rs12169091
NM_006440.5(TXNRD2):c.895A>C (p.Ser299Arg) rs5992495
NM_006440.5(TXNRD2):c.903C>A (p.Thr301=) rs35695986

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