single nucleotide variant | NM_000077.5(CDKN2A):c.458-105A>G | CDKN2A | Pathogenic/Likely pathogenic | 9 | 21968346 | 21968346 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA16612773,OMIM:600160.0014 |
single nucleotide variant | NM_000077.5(CDKN2A):c.457G>T (p.Asp153Tyr) | CDKN2A | Pathogenic/Likely pathogenic | 9 | 21970901 | 21970901 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA337714 |
Indel | NM_000077.5(CDKN2A):c.381_393delinsGATGCG (p.Arg128fs) | CDKN2A | Likely pathogenic | 9 | 21970965 | 21970977 | GCGCAGGTACCGT | CGCATC | criteria provided, single submitter | ClinGen:CA658656022 |
single nucleotide variant | NM_000077.5(CDKN2A):c.377T>A (p.Val126Asp) | CDKN2A | Pathogenic | 9 | 21970981 | 21970981 | A | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA120398,UniProtKB:P42771#VAR_001479,OMIM:600160.0013 |
Duplication | NM_000077.5(CDKN2A):c.359_360dup (p.Leu121fs) | CDKN2A | Likely pathogenic | 9 | 21970997 | 21970998 | G | GCT | criteria provided, single submitter | - |
Deletion | NM_000077.5(CDKN2A):c.358del (p.Glu120fs) | CDKN2A | Pathogenic | 9 | 21971000 | 21971000 | TC | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16612781 |
Duplication | NM_000077.5(CDKN2A):c.340_343dup (p.Val115fs) | CDKN2A | Pathogenic | 9 | 21971014 | 21971015 | A | ACGGG | criteria provided, single submitter | ClinGen:CA10578836 |
Deletion | NM_000077.5(CDKN2A):c.340_355del (p.Pro114fs) | CDKN2A | Likely pathogenic | 9 | 21971003 | 21971018 | TCAGCCAGGTCCACGGG | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656026 |
Duplication | NM_000077.5(CDKN2A):c.335_337dup (p.Arg112dup) | CDKN2A | Pathogenic/Likely pathogenic | 9 | 21971020 | 21971021 | A | AGAC | criteria provided, multiple submitters, no conflicts | ClinGen:CA186348 |
single nucleotide variant | NM_000077.5(CDKN2A):c.334C>G (p.Arg112Gly) | CDKN2A | Pathogenic/Likely pathogenic | 9 | 21971024 | 21971024 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA10578837 |