single nucleotide variant | NM_177438.3(DICER1):c.1144G>T (p.Glu382Ter) | DICER1 | Pathogenic | 14 | 95590765 | 95590765 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA10586462 |
single nucleotide variant | NM_177438.3(DICER1):c.996C>A (p.Tyr332Ter) | DICER1 | Pathogenic | 14 | 95590913 | 95590913 | G | T | criteria provided, single submitter | ClinGen:CA10586463 |
Deletion | NM_177438.3(DICER1):c.878_881del (p.Arg293fs) | DICER1 | Pathogenic | 14 | 95592939 | 95592942 | ATCTC | A | reviewed by expert panel | ClinGen:CA10586464 |
single nucleotide variant | NM_177438.3(DICER1):c.745C>T (p.Gln249Ter) | DICER1 | Pathogenic | 14 | 95593075 | 95593075 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA10586465 |
Indel | NM_177438.3(DICER1):c.735-1_741delinsA | DICER1 | Pathogenic/Likely pathogenic | 14 | 95593079 | 95593086 | AGTATACC | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10586466 |
single nucleotide variant | NM_177438.3(DICER1):c.629T>G (p.Leu210Ter) | DICER1 | Pathogenic | 14 | 95595914 | 95595914 | A | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA10586467 |
Indel | NM_177438.3(DICER1):c.2243_2244delinsAA (p.Cys748Ter) | DICER1 | Pathogenic | 14 | 95577666 | 95577667 | GC | TT | criteria provided, multiple submitters, no conflicts | ClinGen:CA10586468 |
Insertion | NM_177438.3(DICER1):c.2243_2244insACTA (p.Cys748Ter) | DICER1 | Pathogenic | 14 | 95577666 | 95577667 | G | GTAGT | criteria provided, multiple submitters, no conflicts | ClinGen:CA10586469 |
single nucleotide variant | NM_177438.3(DICER1):c.2651-2A>G | DICER1 | Pathogenic | 14 | 95574100 | 95574100 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA16614229 |
Deletion | NM_177438.3(DICER1):c.1767del (p.Lys589fs) | DICER1 | Pathogenic | 14 | 95582144 | 95582144 | AC | A | criteria provided, single submitter | ClinGen:CA16614256 |