ClinVar Miner

List of variants in gene TGFBR2 reported as benign

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Total variants: 34
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HGVS dbSNP
GRCh38/hg38 3p24.1(chr3:30634639-30638613)x1
NM_001024847.2(TGFBR2):c.1062C>T (p.Ala354=) rs397516492
NM_001024847.2(TGFBR2):c.1732T>A (p.Ser578Thr) rs112215250
NM_001024847.2(TGFBR2):c.539C>T (p.Thr180Ile) rs727504406
NM_003242.5(TGFBR2):c.*1521G>A rs11466533
NM_003242.5(TGFBR2):c.*1809A>G rs6550008
NM_003242.5(TGFBR2):c.*2065C>T rs11466536
NM_003242.5(TGFBR2):c.*2085T>A rs11466537
NM_003242.5(TGFBR2):c.*2248dupT rs34914516
NM_003242.5(TGFBR2):c.*747C>G rs11466531
NM_003242.5(TGFBR2):c.-128C>G rs2306856
NM_003242.5(TGFBR2):c.1014G>A (p.Thr338=) rs764720370
NM_003242.5(TGFBR2):c.1062C>T (p.Leu354=) rs113194608
NM_003242.5(TGFBR2):c.1119G>A (p.Met373Ile) rs35719192
NM_003242.5(TGFBR2):c.1125C>T (p.Ile375=) rs751663055
NM_003242.5(TGFBR2):c.1159G>A (p.Val387Met) rs35766612
NM_003242.5(TGFBR2):c.1167C>T (p.Asn389=) rs2228048
NM_003242.5(TGFBR2):c.1266A>G (p.Ala422=) rs2228047
NM_003242.5(TGFBR2):c.1458C>T (p.Ser486=) rs139881155
NM_003242.5(TGFBR2):c.1525-7G>A rs377499122
NM_003242.5(TGFBR2):c.1525-8C>T rs11466530
NM_003242.5(TGFBR2):c.1548G>A (p.Thr516=) rs140662877
NM_003242.5(TGFBR2):c.1602G>A (p.Val534=) rs140818646
NM_003242.5(TGFBR2):c.263+7A>G rs1155705
NM_003242.5(TGFBR2):c.264-35T>G rs11466495
NM_003242.5(TGFBR2):c.383delA (p.Lys128Serfs) rs79375991
NM_003242.5(TGFBR2):c.455-4T>A rs11466512
NM_003242.5(TGFBR2):c.571G>A (p.Val191Ile) rs56105708
NM_003242.5(TGFBR2):c.75A>G (p.Pro25=) rs572435149
NM_003242.5(TGFBR2):c.915C>T (p.Leu305=) rs146030104
NM_003242.5(TGFBR2):c.94+16238C>T rs149757320
NM_003242.5(TGFBR2):c.944C>T (p.Thr315Met) rs34833812
NM_003242.5(TGFBR2):c.984C>T (p.His328=) rs193922666
NM_003242.5(TGFBR2):c.999A>G (p.Leu333=) rs2229102

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