ClinVar Miner

List of variants in gene TG reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_003235.5(TG):c.325A>G (p.Ile109Val) rs35301433 0.00350
NM_003235.5(TG):c.3129C>T (p.His1043=) rs112300885 0.00347
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.3583G>A (p.Gly1195Arg) rs138469414 0.00197
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.8202C>T (p.Gly2734=) rs142157473 0.00040
NM_003235.5(TG):c.1389C>T (p.Asn463=) rs145681459 0.00019
NM_003235.5(TG):c.6498T>C (p.Ser2166=) rs200367054 0.00009
NM_003235.5(TG):c.7136G>A (p.Arg2379His) rs377043149 0.00007
NM_003235.5(TG):c.105G>A (p.Glu35=) rs374559000 0.00004
NM_003235.5(TG):c.7647C>T (p.Gly2549=) rs200261320 0.00002
NM_003235.5(TG):c.1777A>C (p.Arg593=)
NM_003235.5(TG):c.2031T>G (p.Pro677=)
NM_003235.5(TG):c.2223G>A (p.Thr741=)
NM_003235.5(TG):c.2223G>T (p.Thr741=) rs779145179
NM_003235.5(TG):c.2442C>T (p.Ser814=)
NM_003235.5(TG):c.246C>T (p.Gly82=)
NM_003235.5(TG):c.2934C>G (p.Pro978=)
NM_003235.5(TG):c.3231C>T (p.Cys1077=)
NM_003235.5(TG):c.3749G>T (p.Arg1250Leu) rs114944116
NM_003235.5(TG):c.3879A>G (p.Gln1293=)
NM_003235.5(TG):c.6621C>A (p.Gly2207=)
NM_003235.5(TG):c.6622C>A (p.Arg2208=)
NM_003235.5(TG):c.6708G>A (p.Pro2236=)
NM_003235.5(TG):c.7143C>A (p.Ser2381=)

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