ClinVar Miner

List of variants in gene TGM6 reported as benign for Spinocerebellar ataxia type 35

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_198994.3(TGM6):c.1968-10C>T rs6036467 0.98682
NM_198994.3(TGM6):c.172A>G (p.Met58Val) rs2076405 0.93204
NM_198994.3(TGM6):c.850+12G>A rs2076404 0.61481
NM_198994.3(TGM6):c.*31T>C rs2076652 0.44571
NM_198994.3(TGM6):c.1968-11C>T rs2076653 0.44564
NM_198994.3(TGM6):c.1476G>A (p.Lys492=) rs2295077 0.26375
NM_198994.3(TGM6):c.789G>A (p.Lys263=) rs6114033 0.13293
NM_198994.3(TGM6):c.1093+5G>A rs6137891 0.07885
NM_198994.3(TGM6):c.477C>T (p.Ser159=) rs16984872 0.03978
NM_198994.3(TGM6):c.422C>A (p.Ala141Glu) rs73894929 0.02857
NM_198994.3(TGM6):c.1342C>T (p.Arg448Trp) rs147979536 0.01429
NM_198994.3(TGM6):c.989+11C>T rs6048684 0.01409
NM_198994.3(TGM6):c.1103G>A (p.Arg368Gln) rs75122556 0.00731
NM_198994.3(TGM6):c.42G>A (p.Ser14=) rs149394698 0.00719
NM_198994.3(TGM6):c.1126G>A (p.Ala376Thr) rs79724097 0.00706
NM_198994.3(TGM6):c.1656C>T (p.Ala552=) rs75601099 0.00634
NM_198994.3(TGM6):c.1657G>A (p.Val553Met) rs74338361 0.00574
NM_198994.3(TGM6):c.12C>G (p.Ile4Met) rs139796716 0.00438
NM_198994.3(TGM6):c.1235G>A (p.Arg412His) rs142679146 0.00410
NM_198994.3(TGM6):c.1580T>A (p.Val527Glu) rs61729226 0.00370
NM_198994.3(TGM6):c.481A>G (p.Ser161Gly) rs141930579 0.00348
NM_198994.3(TGM6):c.*87C>A rs45544131 0.00240
NM_198994.3(TGM6):c.2052G>A (p.Val684=) rs149369357 0.00165
NM_198994.3(TGM6):c.1523G>A (p.Gly508Asp) rs140719871 0.00149
NM_198994.3(TGM6):c.1995G>C (p.Arg665Ser) rs138807504 0.00136
NM_198994.3(TGM6):c.1216G>A (p.Glu406Lys) rs144338465 0.00135
NM_198994.3(TGM6):c.245G>C (p.Gly82Ala) rs144094215 0.00080
NM_198994.3(TGM6):c.555C>T (p.Asp185=) rs144101264 0.00036
NM_198994.3(TGM6):c.1171G>A (p.Val391Met) rs116904482 0.00026
NM_198994.3(TGM6):c.1040C>T (p.Pro347Leu) rs183670042 0.00024
NM_198994.3(TGM6):c.940G>A (p.Val314Met) rs202184911 0.00021
NM_198994.3(TGM6):c.31T>G (p.Trp11Gly) rs141178275 0.00018
NM_198994.3(TGM6):c.883G>A (p.Val295Met) rs200341133 0.00005
NM_198994.3(TGM6):c.992A>G (p.Asn331Ser) rs138323389 0.00004
NM_198994.3(TGM6):c.-36T>C rs371018532
NM_198994.3(TGM6):c.1198A>G (p.Ile400Val) rs552530897
NM_198994.3(TGM6):c.1967+59AG[2] rs60388755

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