ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 74
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000359.3(TGM1):c.726G>A (p.Glu242=) rs35755034 0.04892
NM_000359.3(TGM1):c.366G>A (p.Ser122=) rs17102410 0.03062
NM_000359.3(TGM1):c.1552G>A (p.Val518Met) rs35312232 0.01146
NM_000359.3(TGM1):c.54G>A (p.Gln18=) rs41295336 0.00761
NM_000359.3(TGM1):c.2264C>T (p.Ser755Leu) rs35926651 0.00599
NM_000359.3(TGM1):c.1559A>G (p.Glu520Gly) rs142404759 0.00555
NM_000359.3(TGM1):c.365C>T (p.Ser122Leu) rs141486741 0.00492
NM_000359.3(TGM1):c.168G>A (p.Ala56=) rs79251149 0.00439
NM_000359.3(TGM1):c.125C>A (p.Ser42Tyr) rs41295338 0.00428
NM_000359.3(TGM1):c.1113C>T (p.Ser371=) rs61747601 0.00421
NM_000359.3(TGM1):c.361C>T (p.Arg121Cys) rs80145541 0.00384
NM_000359.3(TGM1):c.1819C>T (p.Arg607Cys) rs2229464 0.00382
NM_000359.3(TGM1):c.2405A>T (p.Asp802Val) rs2228337 0.00273
NM_000359.3(TGM1):c.429C>T (p.Arg143=) rs144989372 0.00239
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.432G>A (p.Gly144=) rs141559048 0.00102
NM_000359.3(TGM1):c.*162C>A rs8193035 0.00079
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.383A>G (p.Glu128Gly) rs138592626 0.00046
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.944G>T (p.Arg315Leu) rs143473912 0.00021
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.1223_1227del (p.Asp408fs) rs398122905 0.00002
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.1146C>A (p.Gly382=) rs1126432
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

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.