ClinVar Miner

List of variants in gene TGFBR1 reported as likely benign by Invitae

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Gene type:
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Total variants: 30
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HGVS dbSNP
NM_004612.4(TGFBR1):c.1104T>G (p.Ala368=) rs1060504426
NM_004612.4(TGFBR1):c.1125A>G (p.Thr375=) rs7861780
NM_004612.4(TGFBR1):c.120C>T (p.Leu40=) rs201267786
NM_004612.4(TGFBR1):c.1218A>G (p.Leu406=) rs757399188
NM_004612.4(TGFBR1):c.1256-9C>A rs200369181
NM_004612.4(TGFBR1):c.1278G>T (p.Leu426=) rs368928967
NM_004612.4(TGFBR1):c.1311A>T (p.Ser437=) rs1554702468
NM_004612.4(TGFBR1):c.1392G>A (p.Leu464=) rs1588598532
NM_004612.4(TGFBR1):c.1497A>G (p.Glu499=) rs200055681
NM_004612.4(TGFBR1):c.207C>T (p.Ser69=) rs145033378
NM_004612.4(TGFBR1):c.408C>T (p.Phe136=) rs773845018
NM_004612.4(TGFBR1):c.415A>G (p.Ile139Val) rs148176750
NM_004612.4(TGFBR1):c.457G>A (p.Val153Ile) rs56014374
NM_004612.4(TGFBR1):c.46G>A (p.Val16Met) rs1021523079
NM_004612.4(TGFBR1):c.49C>T (p.Leu17=) rs878854714
NM_004612.4(TGFBR1):c.528G>A (p.Thr176=) rs190878719
NM_004612.4(TGFBR1):c.52_54GCG[8] (p.Ala26del) rs11466445
NM_004612.4(TGFBR1):c.582A>G (p.Pro194=) rs200679996
NM_004612.4(TGFBR1):c.582A>T (p.Pro194=) rs200679996
NM_004612.4(TGFBR1):c.603T>C (p.Ile201=) rs1326484806
NM_004612.4(TGFBR1):c.606G>A (p.Ala202=) rs201497553
NM_004612.4(TGFBR1):c.705C>G (p.Ser235=) rs1325342802
NM_004612.4(TGFBR1):c.805+10A>G rs1588585657
NM_004612.4(TGFBR1):c.810T>C (p.Asn270=) rs147388628
NM_004612.4(TGFBR1):c.822T>G (p.Thr274=) rs1588590268
NM_004612.4(TGFBR1):c.87G>C (p.Pro29=) rs1246631676
NM_004612.4(TGFBR1):c.888A>G (p.Thr296=) rs201943631
NM_004612.4(TGFBR1):c.98-5T>C rs771169283
NM_004612.4(TGFBR1):c.98-6T>C rs749295577
NM_004612.4(TGFBR1):c.99G>A (p.Ala33=) rs779055286

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