ClinVar Miner

List of variants in gene TG reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_003235.5(TG):c.3313G>A (p.Val1105Ile) rs115670342 0.00443
NM_003235.5(TG):c.6200-7T>A rs79724982 0.00240
NM_003235.5(TG):c.6181G>A (p.Gly2061Arg) rs115436575 0.00198
NM_003235.5(TG):c.6646A>G (p.Ile2216Val) rs138690529 0.00179
NM_003235.5(TG):c.1567T>C (p.Ser523Pro) rs116062097 0.00135
NM_003235.5(TG):c.4537G>T (p.Asp1513Tyr) rs114305064 0.00128
NM_003235.5(TG):c.3139+9G>A rs201582196 0.00048
NM_003235.5(TG):c.2502G>A (p.Pro834=) rs138731686 0.00029
NM_003235.5(TG):c.198C>T (p.Asp66=) rs141082783 0.00025
NM_003235.5(TG):c.6885C>T (p.Asn2295=) rs149348416 0.00022
NM_003235.5(TG):c.5402-8C>T rs374306199 0.00011
NM_003235.5(TG):c.1021G>C (p.Ala341Pro) rs759789389 0.00009
NM_003235.5(TG):c.4443C>T (p.Tyr1481=) rs201691879 0.00008
NM_003235.5(TG):c.2184G>A (p.Thr728=) rs745749489 0.00004
NM_003235.5(TG):c.1212T>C (p.Phe404=)
NM_003235.5(TG):c.1260G>A (p.Gly420=) rs886038526
NM_003235.5(TG):c.132G>A (p.Lys44=)
NM_003235.5(TG):c.2762-4del
NM_003235.5(TG):c.2769C>A (p.Gly923=)
NM_003235.5(TG):c.3001+10G>A rs886038527
NM_003235.5(TG):c.3729G>A (p.Gln1243=)
NM_003235.5(TG):c.4131G>T (p.Val1377=)
NM_003235.5(TG):c.4461C>T (p.Ser1487=)
NM_003235.5(TG):c.478+15G>A rs141561325
NM_003235.5(TG):c.4857C>T (p.Ser1619=)
NM_003235.5(TG):c.5233+5T>A
NM_003235.5(TG):c.5371T>C (p.Leu1791=)
NM_003235.5(TG):c.5751C>T (p.Phe1917=)
NM_003235.5(TG):c.6055+6A>G
NM_003235.5(TG):c.6933T>C (p.Ser2311=)
NM_003235.5(TG):c.7707C>A (p.Ser2569=)
NM_003235.5(TG):c.7893C>T (p.Ala2631=)
NM_003235.5(TG):c.957C>T (p.Cys319=)

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