MLH1 K618del
Gene Variant Detail

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Gene MLH1
Variant K618del
Impact List deletion
Protein Effect loss of function
Gene Variant Descriptions MLH1 K618del results in the deletion of an amino acid in the EXO1-interacting region and C-terminal dimerization domain of the Mlh1 protein at amino acid 618 (PMID: 22753075). K618del (reported as K616del) results in altered subcellular localization, reduced protein expression compared to wild-type Mlh1 in culture (PMID: 21120944), reduced interaction with Pms2 and Exo1 in a yeast two-hybrid assay (PMID: 12810663), and loss of mismatch repair activity in an in vitro assay (PMID: 29520894).
Associated Drug Resistance
Category Variants Paths

MLH1 mutant MLH1 inact mut MLH1 K618del

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Transcript NM_000249.4
gDNA chr3:g.37047639_37047641delAAG
cDNA c.1852_1854delAAG
Protein p.K618del
Source Database RefSeq
Genome Build GRCh38/hg38

Filtering

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  • 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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