single nucleotide variant | NM_000321.3(RB1):c.2325+1G>A | RB1 | Pathogenic | 13 | 49039248 | 49039248 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA388167737 |
Deletion | NM_000321.3(RB1):c.2299_2302del (p.Asn767fs) | RB1 | Pathogenic | 13 | 49039220 | 49039223 | CAAAT | C | criteria provided, single submitter | ClinGen:CA645369595 |
single nucleotide variant | NM_000321.3(RB1):c.2284C>T (p.Gln762Ter) | RB1 | Pathogenic | 13 | 49039206 | 49039206 | C | T | criteria provided, single submitter | - |
Insertion | NM_000321.3(RB1):c.2247_2248insAA (p.Asp750fs) | RB1 | Pathogenic | 13 | 49039169 | 49039170 | T | TAA | criteria provided, single submitter | ClinGen:CA658798152 |
single nucleotide variant | NM_000321.3(RB1):c.2242G>T (p.Glu748Ter) | RB1 | Pathogenic | 13 | 49039164 | 49039164 | G | T | criteria provided, single submitter | ClinGen:CA026433,OMIM:614041.0010 |
Deletion | NC_000013.11:g.(?_48464992)_(48465374_?)del | RB1 | Pathogenic | 13 | 49039128 | 49039510 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_000321.3(RB1):c.2211G>T (p.Glu737Asp) | RB1 | Pathogenic | 13 | 49037971 | 49037971 | G | T | criteria provided, single submitter | ClinGen:CA388167239 |
single nucleotide variant | NM_000321.3(RB1):c.2211G>A (p.Glu737=) | RB1 | Pathogenic | 13 | 49037971 | 49037971 | G | A | criteria provided, single submitter | ClinGen:CA026429,OMIM:614041.0021 |
single nucleotide variant | NM_000321.3(RB1):c.2206C>T (p.Gln736Ter) | RB1 | Pathogenic | 13 | 49037966 | 49037966 | C | T | criteria provided, single submitter | - |
Deletion | NM_000321.3(RB1):c.2194_2197del (p.Pro732fs) | RB1 | Pathogenic | 13 | 49037954 | 49037957 | TCCTC | T | criteria provided, single submitter | ClinGen:CA16614023 |