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Gene MSH6
Variant L396V
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MSH6 L396V lies within the mismatch binding domain of the Msh6 protein (PMID: 17531815). L396V demonstrates proficient mismatch repair activity in an in vitro assay (PMID: 22102614), but has not been fully biochemically characterized and therefore, its effect on Msh6 protein function is unknown.
Associated Drug Resistance
Category Variants Paths

MSH6 mutant MSH6 L396V

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Transcript NM_000179.3
gDNA chr2:g.47799169C>G
cDNA c.1186C>G
Protein p.L396V
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406803.1 chr2:g.47799169C>G c.1186C>G p.L396V RefSeq GRCh38/hg38
NM_001407362.1 chr2:g.47803488T>G c.1186T>G p.L396V RefSeq GRCh38/hg38
NM_001406796.1 chr2:g.47799169C>G c.1186C>G p.L396V RefSeq GRCh38/hg38
NM_001406798.1 chr2:g.47799169C>G c.1186C>G p.L396V RefSeq GRCh38/hg38
NM_001406817.1 chr2:g.47799169C>G c.1186C>G p.L396V RefSeq GRCh38/hg38
NM_000179.2 chr2:g.47799169C>G c.1186C>G p.L396V RefSeq GRCh38/hg38
NM_001406809.1 chr2:g.47799169C>G c.1186C>G p.L396V RefSeq GRCh38/hg38
NM_000179.3 chr2:g.47799169C>G c.1186C>G p.L396V RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.47799169C>G c.1186C>G p.L396V RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.47799169C>G c.1186C>G p.L396V RefSeq GRCh38/hg38
NM_001406808.1 chr2:g.47799169C>G c.1186C>G p.L396V 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