single nucleotide variant | NM_000321.3(RB1):c.2134T>C (p.Cys712Arg) | RB1 | Pathogenic/Likely pathogenic | 13 | 49037894 | 49037894 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA026423,UniProtKB:P06400#VAR_005587,OMIM:614041.0024 |
single nucleotide variant | NM_000321.3(RB1):c.607+1G>T | RB1 | Pathogenic | 13 | 48923160 | 48923160 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA026463,OMIM:614041.0025 |
single nucleotide variant | NM_000321.3(RB1):c.1818T>A (p.Tyr606Ter) | RB1 | Pathogenic | 13 | 49030343 | 49030343 | T | A | criteria provided, single submitter | ClinGen:CA026402,OMIM:614041.0026 |
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.1399C>T (p.Arg467Ter) | RB1 | Pathogenic | 13 | 48954198 | 48954198 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA026376 |
Duplication | NM_000321.3(RB1):c.1585dup (p.Tyr529fs) | RB1 | Pathogenic | 13 | 48955464 | 48955465 | A | AT | criteria provided, single submitter | ClinGen:CA026382 |
Indel | NM_000321.3(RB1):c.2067_2079delinsCAC (p.Gln689fs) | RB1 | Pathogenic | 13 | 49033930 | 49033942 | GAATGAGTATGAA | CAC | criteria provided, single submitter | ClinGen:CA026419 |
single nucleotide variant | NM_000321.3(RB1):c.1960G>A (p.Val654Met) | RB1 | Pathogenic | 13 | 49030485 | 49030485 | G | A | criteria provided, single submitter | ClinGen:CA026413 |
single nucleotide variant | NM_000321.3(RB1):c.1723C>T (p.Gln575Ter) | RB1 | Pathogenic | 13 | 49027156 | 49027156 | C | T | criteria provided, single submitter | ClinGen:CA026397 |
single nucleotide variant | NM_000321.3(RB1):c.1735C>T (p.Arg579Ter) | RB1 | Pathogenic | 13 | 49027168 | 49027168 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA026398 |