Deletion | NM_001114753.3(ENG):c.408del (p.Glu137fs) | ENG | Likely pathogenic | 9 | 130588904 | 130588904 | CT | C | criteria provided, single submitter | ClinGen:CA658797296 |
Deletion | NM_001114753.3(ENG):c.896_991+90del | ENG | Likely pathogenic | 9 | 130586989 | 130587174 | GCCCAAGCTCACACAGAGGTGCTTCACCAACAGTGTGGCCACTGATCCAAGGGAGGGGAAGGGAAGGGAGGGGCAGGGGAAGGGTGCTCACCGCAGCTGGAGGCATGAAGTGAGACAATGCTGGCCAGCGGTAGCTCCACGAAGGATGCCACAATGCTGGCATTGAGCATCCGGGCCTCCCCCAGGA | G | criteria provided, single submitter | ClinGen:CA658797291 |
single nucleotide variant | NM_005359.6(SMAD4):c.250-2A>G | SMAD4 | Likely pathogenic | 18 | 48575054 | 48575054 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA402458160 |
single nucleotide variant | NM_005359.6(SMAD4):c.905-1G>A | SMAD4 | Likely pathogenic | 18 | 48586235 | 48586235 | G | A | criteria provided, single submitter | ClinGen:CA402463631 |
single nucleotide variant | NM_000020.3(ACVRL1):c.148T>C (p.Trp50Arg) | ACVRL1 | Likely pathogenic | 12 | 52306969 | 52306969 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA384897700 |
Duplication | NC_000009.11:g.(?_130586563)_(130592126_?)dup | ENG | Likely pathogenic | 9 | 130586563 | 130592126 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_001114753.3(ENG):c.1220G>A (p.Ser407Asn) | ENG | Likely pathogenic | 9 | 130582231 | 130582231 | C | T | criteria provided, single submitter | ClinGen:CA374978426 |
single nucleotide variant | NM_000020.3(ACVRL1):c.1270C>T (p.Pro424Ser) | ACVRL1 | Likely pathogenic | 12 | 52312792 | 52312792 | C | T | criteria provided, single submitter | ClinGen:CA384903729 |
single nucleotide variant | NM_001114753.3(ENG):c.781T>G (p.Trp261Gly) | ENG | Likely pathogenic | 9 | 130587545 | 130587545 | A | C | criteria provided, single submitter | ClinGen:CA374983206 |
single nucleotide variant | NM_000020.3(ACVRL1):c.1048+2T>G | ACVRL1 | Likely pathogenic | 12 | 52309286 | 52309286 | T | G | criteria provided, single submitter | ClinGen:CA384901886 |