Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
| Gene | MLH1 |
| Variant | P654L |
| Impact List | missense |
| Protein Effect | loss of function |
| Gene Variant Descriptions | MLH1 P654L lies within the C-terminal dimerization domain of the Mlh1 protein (PMID: 22753075). P654L confers a loss of function to the Mlh1 protein as indicated by a loss of mismatch repair activity (MMR) in an in vitro assay (PMID: 20020535, PMID: 17510385), altered subcellular localization, and reduced protein expression compared to wild-type in cultured cells (PMID: 21120944). |
| Associated Drug Resistance | |
| Category Variants Paths |
MLH1 mutant MLH1 inact mut MLH1 P654L |
| Transcript | NM_000249.4 |
| gDNA | chr3:g.37048581C>T |
| cDNA | c.1961C>T |
| Protein | p.P654L |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000249 | chr3:g.37048581C>T | c.1961C>T | p.P654L | RefSeq | GRCh38/hg38 |
| NM_000249.3 | chr3:g.37048581C>T | c.1961C>T | p.P654L | RefSeq | GRCh38/hg38 |
| NM_001354630.2 | chr3:g.37050508C>T | c.1961C>T | p.P654L | RefSeq | GRCh38/hg38 |
| NM_000249.4 | chr3:g.37048581C>T | c.1961C>T | p.P654L | RefSeq | GRCh38/hg38 |
| NM_001354630.1 | chr3:g.37050508C>T | c.1961C>T | p.P654L | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|