ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 65
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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.2443G>A (p.Gly815Arg) rs16904774 0.03645
NM_003235.5(TG):c.6669G>A (p.Lys2223=) rs61743268 0.01777
NM_003235.5(TG):c.1543C>G (p.Gln515Glu) rs180222 0.01589
NM_003235.5(TG):c.3313G>A (p.Val1105Ile) rs115670342 0.00443
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.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.7737T>C (p.Ala2579=) rs145611717 0.00098
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.3001+6T>G rs372517082 0.00024
NM_003235.5(TG):c.6885C>T (p.Asn2295=) rs149348416 0.00022
NM_003235.5(TG):c.4862C>A (p.Thr1621Lys) rs112003182 0.00016
NM_003235.5(TG):c.4982G>A (p.Arg1661His) rs115509019 0.00012
NM_003235.5(TG):c.1628C>G (p.Thr543Ser) rs763864684 0.00011
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.7640T>A (p.Leu2547Gln) rs2979042 0.00008
NM_003235.5(TG):c.2184G>A (p.Thr728=) rs745749489 0.00004
NM_003235.5(TG):c.925A>G (p.Thr309Ala) rs199712883 0.00002
NM_003235.5(TG):c.1205C>G (p.Ala402Gly)
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.184C>A (p.Gln62Lys)
NM_003235.5(TG):c.2200T>G (p.Ser734Ala) rs180223
NM_003235.5(TG):c.2719G>C (p.Glu907Gln)
NM_003235.5(TG):c.2762-4del
NM_003235.5(TG):c.2769C>A (p.Gly923=)
NM_003235.5(TG):c.2963G>C (p.Arg988Pro) rs16893332
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.5729_5730del (p.Thr1910fs)
NM_003235.5(TG):c.5751C>T (p.Phe1917=)
NM_003235.5(TG):c.5976-2A>C
NM_003235.5(TG):c.6055+6A>G
NM_003235.5(TG):c.6209A>G (p.Asn2070Ser)
NM_003235.5(TG):c.6623G>A (p.Arg2208Gln)
NM_003235.5(TG):c.6933T>C (p.Ser2311=)
NM_003235.5(TG):c.7707C>A (p.Ser2569=)
NM_003235.5(TG):c.7847A>T (p.Asn2616Ile) rs10091530
NM_003235.5(TG):c.7893C>T (p.Ala2631=)
NM_003235.5(TG):c.957C>T (p.Cys319=)

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