ClinVar Miner

List of variants in gene TGM1 reported as benign for not provided

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Gene type:
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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_000359.3(TGM1):c.508+439T>C rs2748516 0.92219
NM_000359.3(TGM1):c.509-196T>G rs7151201 0.15537
NM_000359.3(TGM1):c.1928-47T>G rs8193032 0.13279
NM_000359.3(TGM1):c.2088+72G>A rs8193033 0.10735
NM_000359.3(TGM1):c.1403-273C>G rs3783442 0.05795
NM_000359.3(TGM1):c.726G>A (p.Glu242=) rs35755034 0.04892
NM_000359.3(TGM1):c.1491+54C>T rs3742506 0.04003
NM_000359.3(TGM1):c.366G>A (p.Ser122=) rs17102410 0.03062
NM_000359.3(TGM1):c.1492-51A>G rs2273303 0.02960
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.285C>T (p.Ser95=) rs2228336 0.00581
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.1645+5C>A rs187575724 0.00468
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.1927+20C>T rs41293816 0.00386
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.320-18G>A rs200802924 0.00322
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.920G>A (p.Arg307Gln) rs146770534 0.00155
NM_000359.3(TGM1):c.1298+9G>A rs201015655 0.00140
NM_000359.3(TGM1):c.411C>T (p.Asp137=) rs145002586 0.00113
NM_000359.3(TGM1):c.432G>A (p.Gly144=) rs141559048 0.00102
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.2160C>T (p.Thr720=) rs139387079 0.00040
NM_000359.3(TGM1):c.2258G>A (p.Arg753His) rs202020907 0.00029
NM_000359.3(TGM1):c.167C>T (p.Ala56Val) rs147479810 0.00024
NM_000359.3(TGM1):c.319+8C>T rs41295342 0.00021
NM_000359.3(TGM1):c.885C>T (p.His295=) rs186352813 0.00012
NM_000359.3(TGM1):c.297A>G (p.Ala99=) rs41295340 0.00010
NM_000359.3(TGM1):c.177C>T (p.Asp59=) rs8193031 0.00009
NM_000359.3(TGM1):c.66G>A (p.Thr22=) rs756448718 0.00006
NM_000359.3(TGM1):c.2220C>T (p.Asn740=) rs554951371 0.00002
NM_000359.3(TGM1):c.*96GGGGAGTCCAGGGCTCCCGGAG[1] rs41294726
NM_000359.3(TGM1):c.1146C>A (p.Gly382=) rs1126432
NM_000359.3(TGM1):c.1402+16del
NM_000359.3(TGM1):c.1492-12dup rs111506664
NM_000359.3(TGM1):c.1492-5dup rs764745656
NM_000359.3(TGM1):c.2225+19C>T rs137984692
NM_000359.3(TGM1):c.320-41T>A rs2854996

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