Duplication | NM_005359.6(SMAD4):c.1407_1410dup (p.Gly471fs) | SMAD4 | Pathogenic | 18 | 48603104 | 48603105 | A | ATCCC | criteria provided, single submitter | ClinGen:CA658799052 |
Deletion | NM_005359.6(SMAD4):c.1409del (p.Pro470fs) | SMAD4 | Pathogenic | 18 | 48603106 | 48603106 | TC | T | criteria provided, single submitter | ClinGen:CA658799053 |
single nucleotide variant | NM_005359.6(SMAD4):c.454+2T>C | SMAD4 | Likely pathogenic | 18 | 48575696 | 48575696 | T | C | criteria provided, single submitter | ClinGen:CA402459644 |
Deletion | NM_005359.6(SMAD4):c.955+1del | SMAD4 | Likely pathogenic | 18 | 48586286 | 48586286 | TG | T | criteria provided, single submitter | ClinGen:CA658799061 |
Duplication | NM_004329.3(BMPR1A):c.40dup (p.Tyr14fs) | BMPR1A | Pathogenic/Likely pathogenic | 10 | 88635814 | 88635815 | C | CT | criteria provided, multiple submitters, no conflicts | - |
Indel | NM_004329.3(BMPR1A):c.987_992delinsTGTA (p.Arg329fs) | BMPR1A | Pathogenic | 10 | 88679047 | 88679052 | AGCCCT | TGTA | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_005359.6(SMAD4):c.1308+2T>C | SMAD4 | Pathogenic | 18 | 48593559 | 48593559 | T | C | criteria provided, single submitter | - |
single nucleotide variant | NM_005359.6(SMAD4):c.1523G>A (p.Gly508Asp) | SMAD4 | Likely pathogenic | 18 | 48604701 | 48604701 | G | A | criteria provided, single submitter | - |
Deletion | NM_004329.3(BMPR1A):c.-547_-268+1del | BMPR1A | Pathogenic | 10 | 88516395 | 88516675 | CGGCGGCCGCTGCAGAGATTGGAATCCGCCTGCCGGGCTTGGCGAAGGAGAAGGGAGGAGGCAGGAGCGAGGAGGGAGGAGGGCCAAGGGCGGGCAGGAAGGCTTAGGCTCGGCGCGTCCGTCCGCGCGCGGCGAAGATCGCACGGCCCGATCGAGGGGCGACCGGGTCGGGGCCGCTGCACGCCAAGGGCGAAGGCCGATTCGGGCCCCACTTCGCCCCGGCGGCTCGCCGCGCCCACCCGCTCCGCGCCGAGGGCTGGAGGATGCGTTCCCTGGGGTCCG | C | criteria provided, single submitter | - |
Deletion | NM_004329.3(BMPR1A):c.133_134del (p.Glu45fs) | BMPR1A | Pathogenic | 10 | 88649883 | 88649884 | CAG | C | criteria provided, single submitter | - |