single nucleotide variant | NM_000455.5(STK11):c.921-2A>T | STK11 | Pathogenic | 19 | 1222982 | 1222982 | A | T | criteria provided, single submitter | ClinGen:CA023361 |
single nucleotide variant | NM_000455.5(STK11):c.920+1G>A | STK11 | Pathogenic/Likely pathogenic | 19 | 1222006 | 1222006 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA402951344 |
Deletion | NM_000455.5(STK11):c.920+1del | STK11 | Pathogenic | 19 | 1222005 | 1222005 | AG | A | criteria provided, single submitter | - |
Indel | NM_000455.4(STK11):c.918_919delinsTCC (p.Ser307fs) | STK11 | Pathogenic | 19 | 1222003 | 1222004 | CA | TCC | criteria provided, single submitter | ClinGen:CA658799093 |
single nucleotide variant | NM_000455.5(STK11):c.913C>T (p.Gln305Ter) | STK11 | Pathogenic | 19 | 1221998 | 1221998 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA402951315 |
single nucleotide variant | NM_000455.5(STK11):c.911G>C (p.Arg304Pro) | STK11 | Pathogenic | 19 | 1221996 | 1221996 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA402951309 |
single nucleotide variant | NM_000455.5(STK11):c.910C>T (p.Arg304Trp) | STK11 | Pathogenic | 19 | 1221995 | 1221995 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA023348 |
Deletion | NM_000455.5(STK11):c.910del (p.Arg304fs) | STK11 | Pathogenic | 19 | 1221994 | 1221994 | TC | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16620754 |
single nucleotide variant | NM_000455.5(STK11):c.904C>T (p.Gln302Ter) | STK11 | Pathogenic | 19 | 1221989 | 1221989 | C | T | criteria provided, single submitter | ClinGen:CA402951286 |
Deletion | NM_000455.5(STK11):c.899del (p.Ile300fs) | STK11 | Pathogenic | 19 | 1221984 | 1221984 | AT | A | criteria provided, single submitter | ClinGen:CA023335 |