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Gene | CDKN2A |
Variant | A76T |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | CDKN2A A76T does not lie within any known functional domains of the Cdkn2a protein (UniProt.org). A76T has been identified in sequencing studies (PMID: 31004019, PMID: 26164066, PMID: 34915860), but has not been biochemically characterized and therefore, its effect on Cdkn2a protein function is unknown (PubMed, Oct 2024). |
Associated Drug Resistance | |
Category Variants Paths |
CDKN2A mutant CDKN2A A76T |
Transcript | NM_000077.5 |
gDNA | chr9:g.21971133C>T |
cDNA | c.226G>A |
Protein | p.A76T |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011517676.2 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_011517675.3 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_047422596.1 | chr9:g.21970980C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_058195 | chr9:g.21971176C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_000077.4 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_005251343 | chr9:g.21970980C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_000077.5 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_011517675 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_011517679.1 | chr9:g.21970980C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_000077 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_011517675.2 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_011517679 | chr9:g.21970980C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_047422598.1 | chr9:g.21970980C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_011517676 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_001195132 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_058195.3 | chr9:g.21971176C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_011517676.3 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_047422597.1 | chr9:g.21970980C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_001363763.2 | chr9:g.21970980C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_001195132.1 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
XM_005251343.1 | chr9:g.21970980C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_058195.4 | chr9:g.21971176C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
NM_001195132.2 | chr9:g.21971133C>T | c.226G>A | p.A76T | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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