Deletion | NM_000321.3(RB1):c.2520+1del | RB1 | Pathogenic | 13 | 49047524 | 49047524 | CG | C | criteria provided, single submitter | OMIM:614041.0001,ClinGen:CA256698 |
single nucleotide variant | NM_000321.3(RB1):c.2513C>G (p.Ser838Ter) | RB1 | Pathogenic | 13 | 49047519 | 49047519 | C | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000321.3(RB1):c.2513C>A (p.Ser838Ter) | RB1 | Pathogenic | 13 | 49047519 | 49047519 | C | A | criteria provided, single submitter | ClinGen:CA388168153 |
single nucleotide variant | NM_000321.3(RB1):c.2501C>A (p.Ser834Ter) | RB1 | Pathogenic | 13 | 49047507 | 49047507 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA388168125 |
Deletion | NM_000321.3(RB1):c.2490-1_2490del | RB1 | Pathogenic | 13 | 49047494 | 49047495 | CAG | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000321.3(RB1):c.2490-1398A>G | RB1 | Pathogenic | 13 | 49046098 | 49046098 | A | G | criteria provided, single submitter | ClinGen:CA026441,OMIM:614041.0028 |
single nucleotide variant | NM_000321.3(RB1):c.2489+2T>C | RB1 | Pathogenic | 13 | 49039506 | 49039506 | T | C | criteria provided, single submitter | ClinGen:CA388168096 |
single nucleotide variant | NM_000321.3(RB1):c.2489+1G>A | RB1 | Pathogenic | 13 | 49039505 | 49039505 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA035748 |
single nucleotide variant | NM_000321.3(RB1):c.2489+1G>C | RB1 | Pathogenic | 13 | 49039505 | 49039505 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA10605763 |
Deletion | NM_000321.3(RB1):c.2488_2489+7del | RB1 | Pathogenic | 13 | 49039503 | 49039511 | AAGGTGTGTG | A | criteria provided, single submitter | ClinGen:CA483740435 |