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Gene | MLH1 |
Variant | L588P |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | MLH1 L588P lies within the EXO1-interacting region and C-terminal dimerization domain of the Mlh1 protein (PMID: 22753075). L588P results in defective mismatch repair (MMR) activity in a functional screen in cultured mouse cells (PMID: 31784484) and decreased MMR activity in an in vitro assay (PMID: 17510385). |
Associated Drug Resistance | |
Category Variants Paths |
MLH1 mutant MLH1 inact mut MLH1 L588P |
Transcript | NM_000249.4 |
gDNA | chr3:g.37047550T>C |
cDNA | c.1763T>C |
Protein | p.L588P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001354628.2 | chr3:g.37047550T>C | c.1763T>C | p.L588P | RefSeq | GRCh38/hg38 |
NM_000249.4 | chr3:g.37047550T>C | c.1763T>C | p.L588P | RefSeq | GRCh38/hg38 |
NM_000249.3 | chr3:g.37047550T>C | c.1763T>C | p.L588P | RefSeq | GRCh38/hg38 |
NM_001354628.1 | chr3:g.37047550T>C | c.1763T>C | p.L588P | RefSeq | GRCh38/hg38 |
NM_001258271.1 | chr3:g.37047550T>C | c.1763T>C | p.L588P | RefSeq | GRCh38/hg38 |
NM_001258271.2 | chr3:g.37047550T>C | c.1763T>C | p.L588P | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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