ClinVar Miner

List of variants in gene TGFBR2 reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_003242.6(TGFBR2):c.1062C>T (p.Leu354=) rs113194608 0.00194
NM_003242.6(TGFBR2):c.1119G>A (p.Met373Ile) rs35719192 0.00130
NM_003242.6(TGFBR2):c.106A>G (p.Met36Val) rs17025864 0.00092
NM_003242.6(TGFBR2):c.1458C>T (p.Ser486=) rs139881155 0.00075
NM_003242.6(TGFBR2):c.915C>T (p.Leu305=) rs146030104 0.00026
NM_003242.6(TGFBR2):c.1548G>A (p.Thr516=) rs140662877 0.00021
NM_003242.6(TGFBR2):c.678C>T (p.Asp226=) rs147111149 0.00019
NM_003242.6(TGFBR2):c.984C>T (p.His328=) rs193922666 0.00018
NM_003242.6(TGFBR2):c.1356G>T (p.Leu452=) rs997766869 0.00011
NM_003242.6(TGFBR2):c.1092T>C (p.Asp364=) rs149195553 0.00010
NM_003242.6(TGFBR2):c.577C>T (p.Arg193Trp) rs61762550 0.00008
NM_003242.6(TGFBR2):c.1464G>A (p.Lys488=) rs753282415 0.00007
NM_003242.6(TGFBR2):c.570C>T (p.Arg190=) rs143775631 0.00006
NM_003242.6(TGFBR2):c.985G>A (p.Ala329Thr) rs148665451 0.00006
NM_003242.6(TGFBR2):c.567C>T (p.Tyr189=) rs371221124 0.00005
NM_003242.6(TGFBR2):c.126C>T (p.Asn42=) rs574133875 0.00004
NM_003242.6(TGFBR2):c.1569C>T (p.His523=) rs760107571 0.00004
NM_003242.6(TGFBR2):c.609C>T (p.Thr203=) rs769938385 0.00004
NM_003242.6(TGFBR2):c.696C>T (p.Ala232=) rs768508812 0.00004
NM_003242.6(TGFBR2):c.69G>T (p.Thr23=) rs878854612 0.00004
NM_003242.6(TGFBR2):c.975C>T (p.Thr325=) rs532098604 0.00004
NM_003242.6(TGFBR2):c.1470C>T (p.Asn490=) rs141113059 0.00003
NM_003242.6(TGFBR2):c.1473G>A (p.Val491=) rs752287982 0.00003
NM_003242.6(TGFBR2):c.1680C>T (p.Asp560=) rs376815143 0.00003
NM_003242.6(TGFBR2):c.276C>T (p.Asp92=) rs774840447 0.00003
NM_003242.6(TGFBR2):c.639C>T (p.Ser213=) rs200332401 0.00003
NM_003242.6(TGFBR2):c.690G>A (p.Thr230=) rs201560560 0.00003
NM_003242.6(TGFBR2):c.708C>T (p.Asn236=) rs141554621 0.00003
NM_003242.6(TGFBR2):c.1158C>T (p.Leu386=) rs757158964 0.00002
NM_003242.6(TGFBR2):c.927G>A (p.Thr309=) rs756625146 0.00002
NM_003242.6(TGFBR2):c.1014G>A (p.Thr338=) rs764720370 0.00001
NM_003242.6(TGFBR2):c.1116G>A (p.Lys372=) rs753782498 0.00001
NM_003242.6(TGFBR2):c.1125C>T (p.Ile375=) rs751663055 0.00001
NM_003242.6(TGFBR2):c.1208G>A (p.Arg403His) rs143095746 0.00001
NM_003242.6(TGFBR2):c.1210C>T (p.Leu404=) rs1253996257 0.00001
NM_003242.6(TGFBR2):c.1263T>G (p.Thr421=) rs1397322686 0.00001
NM_003242.6(TGFBR2):c.1293A>G (p.Glu431=) rs774384466 0.00001
NM_003242.6(TGFBR2):c.1314T>C (p.Asn438=) rs772490613 0.00001
NM_003242.6(TGFBR2):c.1482T>C (p.Asp494=) rs757583727 0.00001
NM_003242.6(TGFBR2):c.1644G>A (p.Ser548=) rs781309781 0.00001
NM_003242.6(TGFBR2):c.1659G>A (p.Ser553=) rs771926828 0.00001
NM_003242.6(TGFBR2):c.1701A>G (p.Lys567=) rs763371077 0.00001
NM_003242.6(TGFBR2):c.594T>C (p.Ser198=) rs886038945 0.00001
NM_003242.6(TGFBR2):c.610G>A (p.Gly204Ser) rs773431795 0.00001
NM_003242.6(TGFBR2):c.658C>T (p.Leu220=) rs1424646103 0.00001
NM_003242.6(TGFBR2):c.6T>C (p.Gly2=) rs758864131 0.00001
NM_003242.6(TGFBR2):c.75A>G (p.Pro25=) rs572435149 0.00001
NM_003242.6(TGFBR2):c.810G>A (p.Gln270=) rs777990831 0.00001
NM_003242.6(TGFBR2):c.1039C>T (p.Leu347=)
NM_003242.6(TGFBR2):c.1047G>A (p.Lys349=)
NM_003242.6(TGFBR2):c.1077T>C (p.Ala359=)
NM_003242.6(TGFBR2):c.1080C>T (p.His360=)
NM_003242.6(TGFBR2):c.1137C>T (p.Asp379=) rs1411787654
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.1170C>T (p.Asp390=) rs1699359494
NM_003242.6(TGFBR2):c.12G>A (p.Gly4=)
NM_003242.6(TGFBR2):c.1335C>T (p.Thr445=) rs546058122
NM_003242.6(TGFBR2):c.1338T>C (p.Asp446=)
NM_003242.6(TGFBR2):c.1380C>G (p.Arg460=)
NM_003242.6(TGFBR2):c.1386T>C (p.Asn462=)
NM_003242.6(TGFBR2):c.1474T>C (p.Leu492=)
NM_003242.6(TGFBR2):c.1483C>A (p.Arg495=)
NM_003242.6(TGFBR2):c.1572C>T (p.Asp524=) rs2125455254
NM_003242.6(TGFBR2):c.159T>C (p.Phe53=)
NM_003242.6(TGFBR2):c.15G>T (p.Leu5=)
NM_003242.6(TGFBR2):c.1674T>G (p.Pro558=)
NM_003242.6(TGFBR2):c.198C>G (p.Ser66=)
NM_003242.6(TGFBR2):c.202A>C (p.Met68Leu) rs1060501985
NM_003242.6(TGFBR2):c.240A>G (p.Pro80=) rs2125404896
NM_003242.6(TGFBR2):c.297A>G (p.Thr99=) rs727504343
NM_003242.6(TGFBR2):c.306T>C (p.His102=)
NM_003242.6(TGFBR2):c.393G>A (p.Glu131=)
NM_003242.6(TGFBR2):c.470A>G (p.Asn157Ser)
NM_003242.6(TGFBR2):c.54G>A (p.Thr18=) rs139456857
NM_003242.6(TGFBR2):c.588G>A (p.Lys196=) rs1699342472
NM_003242.6(TGFBR2):c.747G>A (p.Leu249=) rs772907386
NM_003242.6(TGFBR2):c.798C>T (p.Asn266=)
NM_003242.6(TGFBR2):c.897G>A (p.Leu299=) rs1699350239
NM_003242.6(TGFBR2):c.924G>A (p.Leu308=)
NM_003242.6(TGFBR2):c.930T>C (p.Ala310=) rs1341666511
NM_003242.6(TGFBR2):c.948G>A (p.Glu316=) rs1699352075
NM_003242.6(TGFBR2):c.949T>C (p.Leu317=)
NM_003242.6(TGFBR2):c.954G>A (p.Gly318=)

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