ClinVar Miner

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

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Gene type:
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Total variants: 90
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HGVS dbSNP
NM_003242.6(TGFBR2):c.1048C>T (p.Leu350=)
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.1116G>A (p.Lys372=) rs753782498
NM_003242.6(TGFBR2):c.1119G>A (p.Met373Ile) rs35719192
NM_003242.6(TGFBR2):c.1125C>T (p.Ile375=) rs751663055
NM_003242.6(TGFBR2):c.1137C>T (p.Asp379=)
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.1170C>T (p.Asp390=)
NM_003242.6(TGFBR2):c.1208G>A (p.Arg403His) rs143095746
NM_003242.6(TGFBR2):c.1210C>T (p.Leu404=)
NM_003242.6(TGFBR2):c.1239G>T (p.Leu413=)
NM_003242.6(TGFBR2):c.1255-15C>G rs563937625
NM_003242.6(TGFBR2):c.1255-4A>G
NM_003242.6(TGFBR2):c.126C>T (p.Asn42=) rs574133875
NM_003242.6(TGFBR2):c.1335C>T (p.Thr445=) rs546058122
NM_003242.6(TGFBR2):c.1356G>T (p.Leu452=)
NM_003242.6(TGFBR2):c.1392G>A (p.Val464=)
NM_003242.6(TGFBR2):c.1397-11T>C
NM_003242.6(TGFBR2):c.1407T>C (p.Asp469=)
NM_003242.6(TGFBR2):c.1452C>G (p.Val484=)
NM_003242.6(TGFBR2):c.1464G>A (p.Lys488=) rs753282415
NM_003242.6(TGFBR2):c.1473G>A (p.Val491=) rs752287982
NM_003242.6(TGFBR2):c.1482T>C (p.Asp494=)
NM_003242.6(TGFBR2):c.1524+3A>G
NM_003242.6(TGFBR2):c.1525-14C>T
NM_003242.6(TGFBR2):c.1525-6C>G rs748388518
NM_003242.6(TGFBR2):c.1525-7G>A rs377499122
NM_003242.6(TGFBR2):c.1530C>A (p.Ile510=)
NM_003242.6(TGFBR2):c.1539G>A (p.Val513=)
NM_003242.6(TGFBR2):c.1542T>C (p.Cys514=) rs1575166645
NM_003242.6(TGFBR2):c.1548G>A (p.Thr516=) rs140662877
NM_003242.6(TGFBR2):c.1560C>T (p.Cys520=)
NM_003242.6(TGFBR2):c.1569C>T (p.His523=) rs760107571
NM_003242.6(TGFBR2):c.156A>G (p.Lys52=)
NM_003242.6(TGFBR2):c.1626G>A (p.Glu542=) rs375226321
NM_003242.6(TGFBR2):c.1641C>T (p.Leu547=)
NM_003242.6(TGFBR2):c.1644G>A (p.Ser548=)
NM_003242.6(TGFBR2):c.1659G>A (p.Ser553=)
NM_003242.6(TGFBR2):c.1668G>A (p.Lys556=) rs779923854
NM_003242.6(TGFBR2):c.1680C>T (p.Asp560=)
NM_003242.6(TGFBR2):c.207C>T (p.Ser69=) rs1559456575
NM_003242.6(TGFBR2):c.261A>G (p.Val87=)
NM_003242.6(TGFBR2):c.264-11C>T
NM_003242.6(TGFBR2):c.291A>G (p.Leu97=)
NM_003242.6(TGFBR2):c.342A>G (p.Glu114=)
NM_003242.6(TGFBR2):c.455-5A>G rs747104789
NM_003242.6(TGFBR2):c.464C>T (p.Thr155Ile) rs727504406
NM_003242.6(TGFBR2):c.486A>G (p.Leu162=)
NM_003242.6(TGFBR2):c.528G>A (p.Leu176=) rs1303407125
NM_003242.6(TGFBR2):c.54G>A (p.Thr18=)
NM_003242.6(TGFBR2):c.550A>G (p.Ile184Val)
NM_003242.6(TGFBR2):c.558C>T (p.Phe186=)
NM_003242.6(TGFBR2):c.567C>T (p.Tyr189=) rs371221124
NM_003242.6(TGFBR2):c.573T>C (p.Val191=)
NM_003242.6(TGFBR2):c.577C>T (p.Arg193Trp) rs61762550
NM_003242.6(TGFBR2):c.588G>A (p.Lys196=)
NM_003242.6(TGFBR2):c.594T>C (p.Ser198=) rs886038945
NM_003242.6(TGFBR2):c.609C>T (p.Thr203=) rs769938385
NM_003242.6(TGFBR2):c.624G>A (p.Lys208=)
NM_003242.6(TGFBR2):c.633G>A (p.Glu211=)
NM_003242.6(TGFBR2):c.639C>T (p.Ser213=) rs200332401
NM_003242.6(TGFBR2):c.649G>C (p.Ala217Pro) rs149141477
NM_003242.6(TGFBR2):c.658C>T (p.Leu220=)
NM_003242.6(TGFBR2):c.666T>C (p.Asp222=) rs755404252
NM_003242.6(TGFBR2):c.678C>T (p.Asp226=) rs147111149
NM_003242.6(TGFBR2):c.690G>A (p.Thr230=) rs201560560
NM_003242.6(TGFBR2):c.696C>T (p.Ala232=) rs768508812
NM_003242.6(TGFBR2):c.69G>T (p.Thr23=) rs878854612
NM_003242.6(TGFBR2):c.6T>C (p.Gly2=) rs758864131
NM_003242.6(TGFBR2):c.708C>T (p.Asn236=) rs141554621
NM_003242.6(TGFBR2):c.747G>C (p.Leu249=)
NM_003242.6(TGFBR2):c.75A>G (p.Pro25=) rs572435149
NM_003242.6(TGFBR2):c.897G>A (p.Leu299=)
NM_003242.6(TGFBR2):c.915C>T (p.Leu305=) rs146030104
NM_003242.6(TGFBR2):c.927G>A (p.Thr309=) rs756625146
NM_003242.6(TGFBR2):c.933G>A (p.Glu311=) rs754003334
NM_003242.6(TGFBR2):c.94+16245G>A rs61732532
NM_003242.6(TGFBR2):c.94+16256C>T rs143701368
NM_003242.6(TGFBR2):c.948G>A (p.Glu316=)
NM_003242.6(TGFBR2):c.95-7T>C rs764533083
NM_003242.6(TGFBR2):c.95-7T>G
NM_003242.6(TGFBR2):c.975C>T (p.Thr325=) rs532098604
NM_003242.6(TGFBR2):c.978C>T (p.Ala326=) rs1575157891
NM_003242.6(TGFBR2):c.984C>T (p.His328=) rs193922666
NM_003242.6(TGFBR2):c.985G>A (p.Ala329Thr) rs148665451
NM_003242.6(TGFBR2):c.993C>T (p.Gly331=)
NM_003242.6(TGFBR2):c.9G>A (p.Arg3=) rs1559443648

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