Duplication | NM_000321.2(RB1):c.1402_1412dup (p.Gln471Hisfs) | RB1 | Pathogenic | 13 | 48954199 | 48954200 | G | GATTATCCATTC | criteria provided, single submitter | ClinGen:CA275022 |
single nucleotide variant | NM_000321.3(RB1):c.1696-1G>A | RB1 | Pathogenic | 13 | 49027128 | 49027128 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA026395 |
single nucleotide variant | NM_000321.3(RB1):c.2370C>A (p.Tyr790Ter) | RB1 | Pathogenic | 13 | 49039385 | 49039385 | C | A | criteria provided, single submitter | ClinGen:CA026439 |
single nucleotide variant | NM_000321.3(RB1):c.297G>A (p.Trp99Ter) | RB1 | Pathogenic | 13 | 48916767 | 48916767 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA026447 |
single nucleotide variant | NM_000321.3(RB1):c.1154T>G (p.Leu385Ter) | RB1 | Pathogenic | 13 | 48947567 | 48947567 | T | G | criteria provided, single submitter | ClinGen:CA10583158 |
single nucleotide variant | NM_000321.3(RB1):c.1814+3A>C | RB1 | Pathogenic | 13 | 49027250 | 49027250 | A | C | criteria provided, single submitter | ClinGen:CA10583159 |
single nucleotide variant | NM_000321.3(RB1):c.2053C>T (p.Gln685Ter) | RB1 | Pathogenic | 13 | 49033916 | 49033916 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10583160 |
Deletion | NM_000321.3(RB1):c.376del (p.Ile126fs) | RB1 | Pathogenic | 13 | 48916844 | 48916844 | GA | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA10604120 |
single nucleotide variant | NM_000321.3(RB1):c.2548C>T (p.Gln850Ter) | RB1 | Pathogenic | 13 | 49050864 | 49050864 | C | T | criteria provided, single submitter | ClinGen:CA10604891 |
single nucleotide variant | NM_000321.3(RB1):c.1510C>T (p.Gln504Ter) | RB1 | Pathogenic | 13 | 48955394 | 48955394 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10605288 |