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Gene | CDKN2A |
Variant | E119* |
Impact List | nonsense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | CDKN2A E119* results in a premature truncation of the Cdkn2a protein at amino acid 119 of 156 (UniProt.org). E119* has not been characterized, however, due to the effects of other truncation mutations downstream of E119 (PMID: 8668202), is predicted to lead to a loss of Cdkn2a protein function. |
Associated Drug Resistance | |
Category Variants Paths |
CDKN2A mutant CDKN2A inact mut CDKN2A E119* |
Transcript | NM_000077.5 |
gDNA | chr9:g.21971004C>A |
cDNA | c.355G>T |
Protein | p.E119* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000077 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
XM_011517676.3 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
XM_011517676 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
NM_000077.4 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
NM_001195132 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
XM_011517675 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
XM_011517675.2 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
XM_011517675.3 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
NM_001195132.1 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
XM_011517676.2 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
NM_000077.5 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
NM_001195132.2 | chr9:g.21971004C>A | c.355G>T | p.E119* | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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