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Gene | PTEN |
Variant | L112V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | PTEN L112V lies within the phosphatase tensin-type domain of the Pten protein (UniProt.org). L112V has not been biochemically characterized, however, the genomic change leads to activation of a cryptic splice site and aberrant splicing of PTEN (PMID: 18669439). |
Associated Drug Resistance | |
Category Variants Paths |
PTEN mutant PTEN L112V |
Transcript | NM_000314.8 |
gDNA | chr10:g.87933093C>G |
cDNA | c.334C>G |
Protein | p.L112V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001304717.2 | chr10:g.87864284C>G | c.334C>G | p.L112V | RefSeq | GRCh38/hg38 |
NM_000314.8 | chr10:g.87933093C>G | c.334C>G | p.L112V | RefSeq | GRCh38/hg38 |
NM_001304717.5 | chr10:g.87864284C>G | c.334C>G | p.L112V | RefSeq | GRCh38/hg38 |
NM_001304717 | chr10:g.87864284C>G | c.334C>G | p.L112V | RefSeq | GRCh38/hg38 |
NM_000314.6 | chr10:g.87933093C>G | c.334C>G | p.L112V | RefSeq | GRCh38/hg38 |
NM_000314 | chr10:g.87933093C>G | c.334C>G | p.L112V | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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