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Gene | MLH1 |
Variant | L622P |
Impact List | missense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | MLH1 L622P lies within the EXO1-interacting region and C-terminal dimerization domain of the Mlh1 protein (PMID: 22753075). L622P results in reduced methylation sensitivity in culture (PMID: 30998989), and therefore, is predicted to lead to a loss of Mlh1 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
MLH1 mutant MLH1 inact mut MLH1 L622P |
Transcript | NM_000249.4 |
gDNA | chr3:g.37047652T>C |
cDNA | c.1865T>C |
Protein | p.L622P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001258271.2 | chr3:g.37047652T>C | c.1865T>C | p.L622P | RefSeq | GRCh38/hg38 |
NM_000249.4 | chr3:g.37047652T>C | c.1865T>C | p.L622P | RefSeq | GRCh38/hg38 |
NM_001354628.2 | chr3:g.37047652T>C | c.1865T>C | p.L622P | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
MLH1 L622P | loss of function - predicted |