MLH1 E663G
Gene Variant Detail

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Gene MLH1
Variant E663G
Impact List missense
Protein Effect no effect
Gene Variant Descriptions MLH1 E663G lies within the C-terminal dimerization domain of the Mlh1 protein (PMID: 22753075). E663G results in Mlh1 (PMID: 23403630, PMID: 20533529) and Pms2 (PMID: 20533529) protein expression comparable to wild-type in culture and mismatch repair activity comparable to wild-type in yeast assays (PMID: 17510385) and in in vitro assays (PMID: 23403630, PMID: 20533529, PMID: 17510385).
Associated Drug Resistance
Category Variants Paths

MLH1 mutant MLH1 E663G

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Transcript NM_000249.4
gDNA chr3:g.37048608A>G
cDNA c.1988A>G
Protein p.E663G
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000249.4 chr3:g.37048608A>G c.1988A>G p.E663G RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • 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