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Gene MLH1
Variant W666R
Impact List missense
Protein Effect loss of function - predicted
Gene Variant Descriptions MLH1 W666R lies within the C-terminal dimerization domain of the Mlh1 protein (PMID: 22753075). W666R demonstrates no splicing defects (PMID: 18561205) but 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 W666R

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Transcript NM_000249.4
gDNA chr3:g.37048910T>A
cDNA c.1996T>A
Protein p.W666R
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000249.4 chr3:g.37048910T>A c.1996T>A p.W666R RefSeq GRCh38/hg38

Filtering

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  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References