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| Gene | MLH1 |
| Variant | V716M |
| Impact List | missense |
| Protein Effect | no effect |
| Gene Variant Descriptions | MLH1 V716M lies within the C-terminal dimerization domain of the Mlh1 protein (PMID: 22753075). V716M demonstrates reduced Pms2 and Mlh1 expression in culture but has functional mismatch repair activity in culture (PMID: 36054288) and in in vitro analyses, is predicted to be non-pathogenic based on in silico analyses (PMID: 22753075, PMID: 20020535, PMID: 31881334), and results in subcellular localization and protein expression comparable to wild-type (PMID: 21120944). |
| Associated Drug Resistance | |
| Category Variants Paths |
MLH1 mutant MLH1 V716M |
| Transcript | NM_000249.4 |
| gDNA | chr3:g.37050528G>A |
| cDNA | c.2146G>A |
| Protein | p.V716M |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000249 | chr3:g.37050528G>A | c.2146G>A | p.V716M | RefSeq | GRCh38/hg38 |
| NM_000249.4 | chr3:g.37050528G>A | c.2146G>A | p.V716M | RefSeq | GRCh38/hg38 |
| NM_000249.3 | chr3:g.37050528G>A | c.2146G>A | p.V716M | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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