ClinVar Miner

List of variants in gene TGFBR2 reported as likely benign by GeneDx

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Gene type:
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Total variants: 39
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HGVS dbSNP
NC_000003.12:g.30650235T>G
NC_000003.12:g.30688521G>C
NM_001024847.2(TGFBR2):c.118G>A (p.Asp40Asn) rs61732532
NM_001024847.2(TGFBR2):c.136A>C (p.Ser46Arg) rs200111443
NM_003242.5(TGFBR2):c.1525-11delT rs1064795299
NM_003242.5(TGFBR2):c.454+17_454+47del31ins22
NM_003242.6(TGFBR2):c.-31G>A rs767154664
NM_003242.6(TGFBR2):c.1014G>A (p.Thr338=) rs764720370
NM_003242.6(TGFBR2):c.106A>G (p.Met36Val) rs17025864
NM_003242.6(TGFBR2):c.1092T>C (p.Asp364=) rs149195553
NM_003242.6(TGFBR2):c.1128G>A (p.Val376=) rs1057523953
NM_003242.6(TGFBR2):c.1158C>T (p.Leu386=) rs757158964
NM_003242.6(TGFBR2):c.1159G>A (p.Val387Met) rs35766612
NM_003242.6(TGFBR2):c.1159G>T (p.Val387Leu) rs35766612
NM_003242.6(TGFBR2):c.115A>T (p.Thr39Ser) rs780280433
NM_003242.6(TGFBR2):c.1185G>C (p.Leu395=) rs193922663
NM_003242.6(TGFBR2):c.1208G>A (p.Arg403His) rs143095746
NM_003242.6(TGFBR2):c.1254+12C>T rs763098114
NM_003242.6(TGFBR2):c.1254+8A>G rs200630803
NM_003242.6(TGFBR2):c.1397-116G>A
NM_003242.6(TGFBR2):c.1452C>T (p.Val484=) rs185502982
NM_003242.6(TGFBR2):c.1464G>A (p.Lys488=) rs753282415
NM_003242.6(TGFBR2):c.1525-5T>C rs770896804
NM_003242.6(TGFBR2):c.1525-6C>G rs748388518
NM_003242.6(TGFBR2):c.1548G>A (p.Thr516=) rs140662877
NM_003242.6(TGFBR2):c.1569C>T (p.His523=) rs760107571
NM_003242.6(TGFBR2):c.263+17A>C rs34771516
NM_003242.6(TGFBR2):c.263+7_263+9delinsGAC rs1064794518
NM_003242.6(TGFBR2):c.437A>G (p.Asn146Ser) rs863223836
NM_003242.6(TGFBR2):c.454+74A>G
NM_003242.6(TGFBR2):c.455-4T>C rs11466512
NM_003242.6(TGFBR2):c.639C>T (p.Ser213=) rs200332401
NM_003242.6(TGFBR2):c.690G>A (p.Thr230=) rs201560560
NM_003242.6(TGFBR2):c.81C>T (p.His27=) rs1057520957
NM_003242.6(TGFBR2):c.933G>A (p.Glu311=) rs754003334
NM_003242.6(TGFBR2):c.94+16202A>G rs375610471
NM_003242.6(TGFBR2):c.94+16308T>C rs770994456
NM_003242.6(TGFBR2):c.944C>T (p.Thr315Met) rs34833812
NM_003242.6(TGFBR2):c.95-20A>G rs371326218

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