single nucleotide variant | NM_000321.3(RB1):c.1049+3A>G | RB1 | Pathogenic | 13 | 48941742 | 48941742 | A | G | criteria provided, single submitter | - |
single nucleotide variant | NM_000321.3(RB1):c.1498+5G>A | RB1 | Pathogenic | 13 | 48954382 | 48954382 | G | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000321.3(RB1):c.2065C>T (p.Gln689Ter) | RB1 | Pathogenic | 13 | 49033928 | 49033928 | C | T | criteria provided, single submitter | - |
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.2520+5G>T | RB1 | Pathogenic | 13 | 49047531 | 49047531 | G | T | criteria provided, single submitter | - |
Deletion | NC_000013.11:g.(?_48303903)_(48480081_?)del | RB1 | Pathogenic | 13 | 48878039 | 49054217 | na | na | criteria provided, single submitter | - |
Deletion | NC_000013.11:g.(?_48345074)_(48345205_?)del | RB1 | Pathogenic | 13 | 48919210 | 48919341 | na | na | criteria provided, single submitter | - |
Duplication | NM_000321.3(RB1):c.45_70dup (p.Pro24fs) | RB1 | Pathogenic | 13 | 48878088 | 48878089 | G | GCCGCTGCCGCCGCGGAACCCCCGGCA | criteria provided, single submitter | - |
Insertion | NM_000321.3(RB1):c.297_298insA (p.Gly100fs) | RB1 | Pathogenic | 13 | 48916767 | 48916768 | G | GA | criteria provided, single submitter | - |
single nucleotide variant | NM_000321.3(RB1):c.388A>T (p.Lys130Ter) | RB1 | Pathogenic | 13 | 48919223 | 48919223 | A | T | criteria provided, single submitter | - |