ClinVar Miner

List of variants in gene TGM1 reported as uncertain significance by Illumina Laboratory Services, Illumina

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_000359.3(TGM1):c.1552G>A (p.Val518Met) rs35312232 0.01146
NM_000359.3(TGM1):c.125C>A (p.Ser42Tyr) rs41295338 0.00428
NM_000359.3(TGM1):c.61A>G (p.Thr21Ala) rs140542428 0.00149
NM_000359.3(TGM1):c.1298+9G>A rs201015655 0.00140
NM_000359.3(TGM1):c.106C>A (p.Arg36Ser) rs145197904 0.00106
NM_000359.3(TGM1):c.252C>T (p.Gly84=) rs148048398 0.00066
NM_000359.3(TGM1):c.2088+14G>T rs201660106 0.00061
NM_000359.3(TGM1):c.270T>A (p.Pro90=) rs201400055 0.00052
NM_000359.3(TGM1):c.1762G>A (p.Ala588Thr) rs146728175 0.00043
NM_000359.3(TGM1):c.2160C>T (p.Thr720=) rs139387079 0.00040
NM_000359.3(TGM1):c.519C>T (p.Pro173=) rs139811103 0.00028
NM_000359.3(TGM1):c.167C>T (p.Ala56Val) rs147479810 0.00024
NM_000359.3(TGM1):c.463C>T (p.Arg155Trp) rs187901859 0.00016
NM_000359.3(TGM1):c.122G>A (p.Arg41His) rs768398275 0.00015
NM_000359.3(TGM1):c.2221G>A (p.Val741Ile) rs141864003 0.00015
NM_000359.3(TGM1):c.885C>T (p.His295=) rs186352813 0.00012
NM_000359.3(TGM1):c.923G>A (p.Arg308Gln) rs201328637 0.00011
NM_000359.3(TGM1):c.177C>T (p.Asp59=) rs8193031 0.00009
NM_000359.3(TGM1):c.97G>A (p.Gly33Arg) rs142455594 0.00009
NM_000359.3(TGM1):c.1967G>A (p.Arg656Gln) rs369173679 0.00007
NM_000359.3(TGM1):c.838G>A (p.Glu280Lys) rs150181059 0.00007
NM_000359.3(TGM1):c.1761C>T (p.Asp587=) rs751201972 0.00006
NM_000359.3(TGM1):c.550C>T (p.Pro184Ser) rs200517023 0.00006
NM_000359.3(TGM1):c.719G>A (p.Arg240His) rs138574046 0.00006
NM_000359.3(TGM1):c.1062G>A (p.Ala354=) rs758437844 0.00005
NM_000359.3(TGM1):c.*90T>C rs886050437 0.00004
NM_000359.3(TGM1):c.1143T>G (p.Ala381=) rs149449576 0.00004
NM_000359.3(TGM1):c.1317C>T (p.Asn439=) rs141972252 0.00004
NM_000359.3(TGM1):c.1305C>T (p.Phe435=) rs1444157818 0.00003
NM_000359.3(TGM1):c.16C>T (p.Arg6Cys) rs372412279 0.00003
NM_000359.3(TGM1):c.2337C>T (p.His779=) rs755635993 0.00003
NM_000359.3(TGM1):c.1467C>T (p.Tyr489=) rs768561754 0.00002
NM_000359.3(TGM1):c.33T>C (p.Arg11=) rs754885672 0.00002
NM_000359.3(TGM1):c.1403-15C>T rs935571611 0.00001
NM_000359.3(TGM1):c.265C>T (p.Arg89Trp) rs146189995 0.00001
NM_000359.3(TGM1):c.278G>A (p.Arg93Gln) rs753328770 0.00001
NM_000359.3(TGM1):c.359C>T (p.Ser120Leu) rs138885883 0.00001
NM_000359.3(TGM1):c.520G>A (p.Glu174Lys) rs768705863 0.00001
NM_000359.3(TGM1):c.791G>A (p.Arg264Gln) rs781006633 0.00001
NM_000359.3(TGM1):c.959A>G (p.Asn320Ser) rs768214832 0.00001
NM_000359.3(TGM1):c.*164G>A rs978100908
NM_000359.3(TGM1):c.1104G>A (p.Thr368=) rs902231692
NM_000359.3(TGM1):c.1336C>G (p.Pro446Ala) rs886050438
NM_000359.3(TGM1):c.1567A>G (p.Ile523Val) rs1047493777
NM_000359.3(TGM1):c.1940C>T (p.Thr647Ile) rs778371971
NM_000359.3(TGM1):c.1966C>T (p.Arg656Trp) rs144318024
NM_000359.3(TGM1):c.2121T>C (p.Cys707=) rs749407588
NM_000359.3(TGM1):c.2231T>A (p.Ile744Asn) rs767241210
NM_000359.3(TGM1):c.319+15T>C rs886050441
NM_000359.3(TGM1):c.319+9G>A rs749759208
NM_000359.3(TGM1):c.454C>G (p.Leu152Val) rs532525772
NM_000359.3(TGM1):c.566G>A (p.Gly189Asp) rs886050440
NM_000359.3(TGM1):c.631A>G (p.Thr211Ala) rs566962779
NM_000359.3(TGM1):c.641A>G (p.Asn214Ser) rs147994543
NM_000359.3(TGM1):c.901T>C (p.Cys301Arg) rs2040791339
NM_000359.3(TGM1):c.941G>A (p.Gly314Asp) rs886050439

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