ClinVar Miner

List of variants in gene TG studied for not specified

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_003235.5(TG):c.3082A>G (p.Met1028Val) rs853326 0.60247
NM_003235.5(TG):c.2334T>C (p.Pro778=) rs2069550 0.59900
NM_003235.5(TG):c.7589G>A (p.Arg2530Gln) rs1133076 0.56572
NM_003235.5(TG):c.4506T>C (p.Ala1502=) rs853304 0.55069
NM_003235.5(TG):c.7920C>T (p.Tyr2640=) rs2294024 0.49806
NM_003235.5(TG):c.3848-20T>C rs2261147 0.47593
NM_003235.5(TG):c.3935A>G (p.Asp1312Gly) rs2069556 0.47427
NM_003235.5(TG):c.5512G>A (p.Asp1838Asn) rs2069561 0.39534
NM_003235.5(TG):c.5995C>T (p.Arg1999Trp) rs2076740 0.37641
NM_003235.5(TG):c.5921T>C (p.Met1974Thr) rs56230101 0.13536
NM_003235.5(TG):c.6395C>T (p.Ser2132Leu) rs61741457 0.04126
NM_003235.5(TG):c.1543C>G (p.Gln515Glu) rs180222 0.01589
NM_003235.5(TG):c.3187C>A (p.Leu1063Met) rs11992497 0.00903
NM_003235.5(TG):c.325A>G (p.Ile109Val) rs35301433 0.00350
NM_003235.5(TG):c.144C>T (p.Tyr48=) rs114436500 0.00345
NM_003235.5(TG):c.6200-7T>A rs79724982 0.00240
NM_003235.5(TG):c.7083G>T (p.Ala2361=) rs116723711 0.00239
NM_003235.5(TG):c.7665C>T (p.Arg2555=) rs115139074 0.00214
NM_003235.5(TG):c.3583G>A (p.Gly1195Arg) rs138469414 0.00197
NM_003235.5(TG):c.3035C>T (p.Pro1012Leu) rs115936153 0.00159
NM_003235.5(TG):c.1567T>C (p.Ser523Pro) rs116062097 0.00135
NM_003235.5(TG):c.3057C>T (p.Ser1019=) rs116032324 0.00120
NM_003235.5(TG):c.229G>A (p.Gly77Ser) rs142698837 0.00071
NM_003235.5(TG):c.3139+9G>A rs201582196 0.00048
NM_003235.5(TG):c.4527C>T (p.His1509=) rs201216611 0.00039
NM_003235.5(TG):c.8026C>T (p.Arg2676Trp) rs114613744 0.00038
NM_003235.5(TG):c.3174C>T (p.Phe1058=) rs140301550 0.00016
NM_003235.5(TG):c.4797C>T (p.Pro1599=) rs369301609 0.00008
NM_003235.5(TG):c.6563-3C>T rs200211140 0.00006
NM_003235.5(TG):c.6695C>T (p.Pro2232Leu) rs201514086 0.00004
NM_003235.5(TG):c.3397G>A (p.Glu1133Lys) rs375727924 0.00003
NM_003235.5(TG):c.1027G>A (p.Gly343Arg) rs1385670566 0.00001
NM_003235.5(TG):c.1260G>A (p.Gly420=) rs886038526
NM_003235.5(TG):c.2200T>G (p.Ser734Ala) rs180223
NM_003235.5(TG):c.3001+10G>A rs886038527
NM_003235.5(TG):c.3040G>A (p.Asp1014Asn)
NM_003235.5(TG):c.3749G>T (p.Arg1250Leu) rs114944116
NM_003235.5(TG):c.478+15G>A rs141561325
NM_003235.5(TG):c.7997G>A (p.Gly2666Glu)

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