Deletion | NM_000321.3(RB1):c.1024del (p.Thr342fs) | RB1 | Pathogenic | 13 | 48941711 | 48941711 | TA | T | criteria provided, single submitter | ClinGen:CA026358 |
single nucleotide variant | NM_000321.3(RB1):c.1049+1G>A | RB1 | Pathogenic/Likely pathogenic | 13 | 48941740 | 48941740 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA026360 |
single nucleotide variant | NM_000321.3(RB1):c.1216-1G>A | RB1 | Pathogenic | 13 | 48951053 | 48951053 | G | A | criteria provided, single submitter | ClinGen:CA026368 |
single nucleotide variant | NM_000321.3(RB1):c.1332+1G>A | RB1 | Pathogenic | 13 | 48951171 | 48951171 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA026369 |
single nucleotide variant | NM_000321.3(RB1):c.1363C>T (p.Arg455Ter) | RB1 | Pathogenic | 13 | 48953760 | 48953760 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA026373 |
Deletion | NM_000321.3(RB1):c.1456_1457del (p.Leu486fs) | RB1 | Pathogenic | 13 | 48954334 | 48954335 | CTT | C | criteria provided, single submitter | ClinGen:CA026378 |
single nucleotide variant | NM_000321.3(RB1):c.1654C>T (p.Arg552Ter) | RB1 | Pathogenic | 13 | 48955538 | 48955538 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA026383 |
Deletion | NM_000321.3(RB1):c.1421+12_1421+32del | RB1 | Likely pathogenic | 13 | 48954223 | 48954243 | TAAATTTTTTACTTTTAGTAAA | T | criteria provided, single submitter | ClinGen:CA269950 |
Deletion | NM_000321.3(RB1):c.54_79del (p.Glu19fs) | RB1 | Pathogenic | 13 | 48878094 | 48878119 | TGCCGCCGCGGAACCCCCGGCACCGCC | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA026461 |
Deletion | NM_000321.3(RB1):c.1191del (p.Glu398fs) | RB1 | Pathogenic | 13 | 48947604 | 48947604 | CA | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA026366 |