ClinVar Miner

List of variants in gene TGFBR2 reported as uncertain significance for not specified

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Total variants: 24
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HGVS dbSNP
NM_003242.5(TGFBR2):c.1397-157_1397-153delTCTTA rs1279882821
NM_003242.6(TGFBR2):c.-8G>A rs727504344
NM_003242.6(TGFBR2):c.1016G>C (p.Arg339Pro) rs727503473
NM_003242.6(TGFBR2):c.1082_1084del (p.Leu361del) rs727503474
NM_003242.6(TGFBR2):c.1152T>A (p.Asn384Lys) rs193922661
NM_003242.6(TGFBR2):c.1163A>G (p.Lys388Arg) rs193922662
NM_003242.6(TGFBR2):c.116C>A (p.Thr39Asn) rs146277116
NM_003242.6(TGFBR2):c.1185G>C (p.Leu395=) rs193922663
NM_003242.6(TGFBR2):c.118G>A (p.Asp40Asn) rs397516837
NM_003242.6(TGFBR2):c.1282G>C (p.Glu428Gln) rs397516838
NM_003242.6(TGFBR2):c.1418C>A (p.Pro473Gln) rs397516839
NM_003242.6(TGFBR2):c.1441C>T (p.His481Tyr) rs762756916
NM_003242.6(TGFBR2):c.1525-7G>A rs377499122
NM_003242.6(TGFBR2):c.1570G>T (p.Asp524Tyr) rs727504421
NM_003242.6(TGFBR2):c.1580C>T (p.Ala527Val) rs727503476
NM_003242.6(TGFBR2):c.1657T>A (p.Ser553Thr) rs112215250
NM_003242.6(TGFBR2):c.1680C>G (p.Asp560Glu) rs376815143
NM_003242.6(TGFBR2):c.367A>T (p.Met123Leu) rs768385200
NM_003242.6(TGFBR2):c.464C>T (p.Thr155Ile) rs727504406
NM_003242.6(TGFBR2):c.569G>A (p.Arg190His) rs780542125
NM_003242.6(TGFBR2):c.617C>T (p.Thr206Met) rs150022335
NM_003242.6(TGFBR2):c.859T>C (p.Trp287Arg) rs727503472
NM_003242.6(TGFBR2):c.934G>A (p.Glu312Lys) rs397516841
NM_003242.6(TGFBR2):c.985G>A (p.Ala329Thr) rs148665451

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