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Gene | MLH1 |
Variant | S692P |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | MLH1 S692P lies within the C-terminal dimerization domain of the Mlh1 protein (PMID: 22753075). S692P results in reduced expression of Mlh1 and Pms2 but mismatch repair activity comparable to wild-type in culture (PMID: 36054288), but has not been fully biochemically characterized and therefore, its effect on Mlh1 protein function is unknown. |
Associated Drug Resistance | |
Category Variants Paths |
MLH1 mutant MLH1 S692P |
Transcript | NM_000249.4 |
gDNA | chr3:g.37048988T>C |
cDNA | c.2074T>C |
Protein | p.S692P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000249.4 | chr3:g.37048988T>C | c.2074T>C | p.S692P | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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