single nucleotide variant | NM_000321.3(RB1):c.2520+5G>A | RB1 | Pathogenic/Likely pathogenic | 13 | 49047531 | 49047531 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA645369529 |
Duplication | NC_000013.10:g.(?_48916729)_(48942746_?)dup | RB1 | Pathogenic | 13 | 48916729 | 48942746 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_000321.3(RB1):c.861G>C (p.Glu287Asp) | RB1 | Pathogenic | 13 | 48937093 | 48937093 | G | C | criteria provided, single submitter | ClinGen:CA388159722 |
Deletion | NM_000321.3(RB1):c.1458del (p.Leu486fs) | RB1 | Pathogenic | 13 | 48954337 | 48954337 | TA | T | criteria provided, single submitter | ClinGen:CA658656368 |
Deletion | NC_000013.11:g.(?_48307274)_(48349029_?)del | RB1 | Pathogenic | 13 | 48881410 | 48923165 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_000321.3(RB1):c.940-1G>T | RB1 | Pathogenic | 13 | 48941629 | 48941629 | G | T | criteria provided, single submitter | ClinGen:CA388160564 |
Duplication | NM_000321.3(RB1):c.1278dup (p.Lys427Ter) | RB1 | Pathogenic | 13 | 48951113 | 48951114 | C | CT | criteria provided, single submitter | ClinGen:CA658656361 |
single nucleotide variant | NM_000321.3(RB1):c.2489+2T>C | RB1 | Pathogenic | 13 | 49039506 | 49039506 | T | C | criteria provided, single submitter | ClinGen:CA388168096 |
Duplication | NM_000321.3(RB1):c.54_73dup (p.Pro25fs) | RB1 | Pathogenic | 13 | 48878094 | 48878095 | G | GCCGCCGCGGAACCCCCGGCA | criteria provided, single submitter | ClinGen:CA658658234 |
single nucleotide variant | NM_000321.3(RB1):c.1333-2A>G | RB1 | Pathogenic | 13 | 48953728 | 48953728 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA388162526 |