single nucleotide variant | NM_005902.4(SMAD3):c.5C>A (p.Ser2Ter) | SMAD3 | Pathogenic/Likely pathogenic | 15 | 67358497 | 67358497 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA393202677 |
single nucleotide variant | NM_003239.5(TGFB3):c.973C>T (p.Arg325Ter) | TGFB3 | Pathogenic/Likely pathogenic | 14 | 76427373 | 76427373 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA390468002 |
single nucleotide variant | NM_003238.6(TGFB2):c.958C>T (p.Arg320Cys) | TGFB2 | Pathogenic/Likely pathogenic | 1 | 218610710 | 218610710 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA344727446,OMIM:190220.0005 |
Deletion | NM_003239.5(TGFB3):c.1102_1105del (p.Leu368fs) | TGFB3 | Pathogenic/Likely pathogenic | 14 | 76425664 | 76425667 | TTCAG | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA658798230 |
single nucleotide variant | NM_005902.4(SMAD3):c.733G>C (p.Gly245Arg) | SMAD3 | Pathogenic/Likely pathogenic | 15 | 67473653 | 67473653 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA392956090 |
single nucleotide variant | NM_005902.4(SMAD3):c.754C>T (p.Gln252Ter) | SMAD3 | Pathogenic/Likely pathogenic | 15 | 67473674 | 67473674 | C | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_004612.4(TGFBR1):c.1457T>C (p.Leu486Ser) | TGFBR1 | Pathogenic/Likely pathogenic | 9 | 101911532 | 101911532 | T | C | criteria provided, multiple submitters, no conflicts | - |