single nucleotide variant | NM_144997.7(FLCN):c.1657T>C (p.Trp553Arg) | FLCN | Pathogenic/Likely pathogenic | 17 | 17117052 | 17117052 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA398529920 |
Deletion | NM_144997.7(FLCN):c.1607_1622del (p.Leu536fs) | FLCN | Pathogenic | 17 | 17117087 | 17117102 | CGCACCCAGGATGCTCA | C | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_144997.7(FLCN):c.1601del (p.Lys534fs) | FLCN | Pathogenic | 17 | 17117108 | 17117108 | CT | C | criteria provided, single submitter | ClinGen:CA10588639 |
Duplication | NM_144997.7(FLCN):c.1599_1600dup (p.Lys534fs) | FLCN | Pathogenic | 17 | 17117108 | 17117109 | T | TTC | criteria provided, single submitter | ClinGen:CA658656529 |
Deletion | NM_144997.7(FLCN):c.1584del (p.Glu530fs) | FLCN | Pathogenic/Likely pathogenic | 17 | 17117125 | 17117125 | TG | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA645369642 |
Insertion | NM_144997.7(FLCN):c.1579_1580insA (p.Arg527fs) | FLCN | Pathogenic | 17 | 17117129 | 17117130 | C | CT | criteria provided, multiple submitters, no conflicts | ClinGen:CA8415933 |
single nucleotide variant | NM_144997.7(FLCN):c.1579C>T (p.Arg527Ter) | FLCN | Pathogenic/Likely pathogenic | 17 | 17117130 | 17117130 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA10586246 |
Deletion | NM_144997.7(FLCN):c.1578_1599del (p.Ser526fs) | FLCN | Pathogenic/Likely pathogenic | 17 | 17117110 | 17117131 | TCTGTGTGTCCTCTTTGGGTCGA | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16043039 |
single nucleotide variant | NM_144997.7(FLCN):c.1540A>T (p.Lys514Ter) | FLCN | Pathogenic | 17 | 17117169 | 17117169 | T | A | criteria provided, single submitter | ClinGen:CA10603293 |
single nucleotide variant | NM_144997.7(FLCN):c.1539-2A>G | FLCN | Pathogenic/Likely pathogenic | 17 | 17117172 | 17117172 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA10583451 |