Indel | NM_000077.5(CDKN2A):c.202_203delinsTT (p.Ala68Leu) | CDKN2A | Likely pathogenic | 9 | 21971155 | 21971156 | GC | AA | criteria provided, multiple submitters, no conflicts | ClinGen:CA10578845 |
single nucleotide variant | NM_000077.5(CDKN2A):c.212A>G (p.Asn71Ser) | CDKN2A | Likely pathogenic | 9 | 21971146 | 21971146 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA5012207 |
Deletion | NM_000077.5(CDKN2A):c.212del (p.Asn71fs) | CDKN2A | Pathogenic | 9 | 21971146 | 21971146 | GT | G | criteria provided, single submitter | ClinGen:CA10578844 |
Deletion | NM_000077.5(CDKN2A):c.221del (p.Asp74fs) | CDKN2A | Pathogenic | 9 | 21971137 | 21971137 | GT | G | criteria provided, single submitter | - |
Deletion | NM_000077.5(CDKN2A):c.225_243del (p.Ala76fs) | CDKN2A | Pathogenic | 9 | 21971115 | 21971133 | CGGGTCGGGTGAGAGTGGCG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA299023 |
Deletion | NM_000077.5(CDKN2A):c.238del (p.Arg80fs) | CDKN2A | Likely pathogenic | 9 | 21971120 | 21971120 | CG | C | criteria provided, single submitter | - |
single nucleotide variant | NM_000077.5(CDKN2A):c.238C>T (p.Arg80Ter) | CDKN2A | Pathogenic/Likely pathogenic | 9 | 21971120 | 21971120 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA120380,OMIM:600160.0002 |
Deletion | NM_000077.5(CDKN2A):c.240_253del (p.Pro81fs) | CDKN2A | Pathogenic | 9 | 21971105 | 21971118 | GCGTCGTGCACGGGT | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA299024 |
single nucleotide variant | NM_000077.5(CDKN2A):c.249C>G (p.His83Gln) | CDKN2A | Pathogenic | 9 | 21971109 | 21971109 | G | C | criteria provided, single submitter | ClinGen:CA16602820 |
single nucleotide variant | NM_000077.5(CDKN2A):c.259C>T (p.Arg87Trp) | CDKN2A | Likely pathogenic | 9 | 21971099 | 21971099 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA5012197 |