Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_005359.6(SMAD4):c.1139+1G>A | SMAD4 | Likely pathogenic | 18 | 48591977 | 48591977 | G | A | criteria provided, single submitter | - |
single nucleotide variant | NM_005359.6(SMAD4):c.1091T>G (p.Leu364Trp) | SMAD4 | Likely pathogenic | 18 | 48591928 | 48591928 | T | G | criteria provided, single submitter | - |
Deletion | NM_005359.6(SMAD4):c.1088_1090del (p.Cys363del) | SMAD4 | Likely pathogenic | 18 | 48591923 | 48591925 | TTTG | T | criteria provided, single submitter | - |
single nucleotide variant | NM_005359.6(SMAD4):c.989A>G (p.Glu330Gly) | SMAD4 | Likely pathogenic | 18 | 48591826 | 48591826 | A | G | criteria provided, single submitter | ClinGen:CA165407,UniProtKB:Q13485#VAR_022833,UniProtKB/Swiss-Prot:VAR_022833 |
single nucleotide variant | NM_005359.6(SMAD4):c.1081C>A (p.Arg361Ser) | SMAD4 | Likely pathogenic | 18 | 48591918 | 48591918 | C | A | criteria provided, single submitter | ClinGen:CA259197 |
single nucleotide variant | NM_004329.3(BMPR1A):c.1013C>A (p.Ala338Asp) | BMPR1A | Likely pathogenic | 10 | 88679073 | 88679073 | C | A | criteria provided, single submitter | ClinGen:CA254361,UniProtKB:P36894#VAR_015534,OMIM:601299.0005 |