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 | L636P |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | MLH1 L636P lies within the EXO1-interacting region and C-terminal dimerization domain of the Mlh1 protein (PMID: 22753075). L636P retains binding with Pms2 and mismatch repair activity in one study (PMID: 20533529), but results in defective mismatch repair (MMR) activity in a functional screen in cultured mouse cells in another study (PMID: 31784484) and decreased Mlh1 expression in culture (PMID: 20533529), and therefore, its effect on Mlh1 protein function is unknown. |
| Associated Drug Resistance | |
| Category Variants Paths |
MLH1 mutant MLH1 L636P |
| Transcript | NM_000249.4 |
| gDNA | chr3:g.37048527T>C |
| cDNA | c.1907T>C |
| Protein | p.L636P |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000249.3 | chr3:g.37048527T>C | c.1907T>C | p.L636P | RefSeq | GRCh38/hg38 |
| NM_000249.4 | chr3:g.37048527T>C | c.1907T>C | p.L636P | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| MLH1 L636P | unknown |