ClinVar Miner

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

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Total variants: 18
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HGVS dbSNP
NM_001024847.2(TGFBR2):c.118G>A (p.Asp40Asn) rs61732532
NM_001024847.2(TGFBR2):c.129C>T (p.Ile43=) rs143701368
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.1159G>A (p.Val387Met) rs35766612
NM_003242.6(TGFBR2):c.1159G>T (p.Val387Leu) rs35766612
NM_003242.6(TGFBR2):c.1208G>A (p.Arg403His) rs143095746
NM_003242.6(TGFBR2):c.1255-15C>G rs563937625
NM_003242.6(TGFBR2):c.1335C>T (p.Thr445=) rs546058122
NM_003242.6(TGFBR2):c.1525-7G>A rs377499122
NM_003242.6(TGFBR2):c.1626G>A (p.Glu542=) rs375226321
NM_003242.6(TGFBR2):c.207C>T (p.Ser69=) rs1559456575
NM_003242.6(TGFBR2):c.455-5A>G rs747104789
NM_003242.6(TGFBR2):c.528G>A (p.Leu176=) rs1303407125
NM_003242.6(TGFBR2):c.708C>T (p.Asn236=) rs141554621
NM_003242.6(TGFBR2):c.95-7T>C rs764533083
NM_003242.6(TGFBR2):c.984C>T (p.His328=) rs193922666
NM_003242.6(TGFBR2):c.9G>A (p.Arg3=) rs1559443648

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