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Gene | CDKN2A |
Variant | D108N |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | CDKN2A D108N does not lie within any known functional domains of the Cdkn2a protein (UniProt.org). D108N results in reduced stability of Cdkn2a protein and partially reduced ability to displace CDK4, but displaces Cdc37 from CDK6 to similar levels of wild-type Cdkn2a (PMID: 29091774), and therefore, its effect on Cdkn2a protein function is unknown. |
Associated Drug Resistance | |
Category Variants Paths |
CDKN2A mutant CDKN2A D108N |
Transcript | NM_000077.5 |
gDNA | chr9:g.21971037C>T |
cDNA | c.322G>A |
Protein | p.D108N |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001195132 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
NM_001195132.1 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
NM_000077.4 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
NM_001195132.2 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
NM_000077.5 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
XM_011517675.3 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
XM_011517676 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
NM_000077 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
XM_011517675 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
XM_011517675.2 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
XM_011517676.3 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
XM_011517676.2 | chr9:g.21971037C>T | c.322G>A | p.D108N | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|---|---|---|---|---|---|---|
CDKN2A mutant | biliary tract cancer | no benefit | Palbociclib | Phase II | Actionable | In a Phase II trial (TAPUR), patients with biliary cancer harboring a CDKN2A mutation or loss of CDKN2A (n=10) did not demonstrate an objective response or stable disease at 16 weeks when treated with single therapy, Ibrance (palbociclib), demonstrating a median progression-free survival of 7.3 weeks and an overall survival of 11.1 weeks (JCO Precision Oncology, Aug 14, 2019; NCT02693535). | detail... |
CDKN2A mutant | skin melanoma | not applicable | N/A | Guideline | Risk Factor | Germline CDKN2A mutations or polymorphisms are associated with increased risk of developing single or multiple primary cutaneous melanomas (NCCN.org). | detail... |
CDKN2A mutant | pancreatic cancer | no benefit | Palbociclib | Phase II | Actionable | In a Phase II trial (TAPUR), patients with pancreatic cancer harboring a CDKN2A mutation or loss of CDKN2A (n=10) did not demonstrate an objective response or stable disease at 16 weeks when treated with single therapy, Ibrance (palbociclib), demonstrating a median progression-free survival of 7.2 weeks and an overall survival of 12.4 weeks (JCO Precision Oncology, Aug 14, 2019; NCT02693535). | detail... |
CDKN2A mutant | pancreatic cancer | not applicable | N/A | Guideline | Risk Factor | Germline mutations in CDKN2A results in familial malignant melanoma syndrome, which is associated with increased risk of developing pancreatic cancer (NCCN.org). | detail... |