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Gene MSH6
Variant S677T
Impact List missense
Protein Effect no effect - predicted
Gene Variant Descriptions MSH6 S677T lies within the connector domain of the Msh6 protein (PMID: 17531815). S677T results in protein stability in cultured cells and mismatch repair activity in an in vitro assay similar to wild-type Msh6 (PMID: 22581703), and therefore, is predicted to have no effect on Msh6 protein function.
Associated Drug Resistance
Category Variants Paths

MSH6 mutant MSH6 S677T

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Transcript NM_000179.3
gDNA chr2:g.47800013G>C
cDNA c.2030G>C
Protein p.S677T
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406808.1 chr2:g.47800013G>C c.2030G>C p.S677T RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.47800013G>C c.2030G>C p.S677T RefSeq GRCh38/hg38
NM_001406798.1 chr2:g.47800013G>C c.2030G>C p.S677T RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.47800013G>C c.2030G>C p.S677T RefSeq GRCh38/hg38
NM_001406817.1 chr2:g.47805657G>C c.2030G>C p.S677T RefSeq GRCh38/hg38
NM_001406803.1 chr2:g.47800013G>C c.2030G>C p.S677T RefSeq GRCh38/hg38
NM_001406809.1 chr2:g.47800013G>C c.2030G>C p.S677T RefSeq GRCh38/hg38
NM_000179.2 chr2:g.47800013G>C c.2030G>C p.S677T RefSeq GRCh38/hg38
NM_001406796.1 chr2:g.47800013G>C c.2030G>C p.S677T RefSeq GRCh38/hg38
NM_000179.3 chr2:g.47800013G>C c.2030G>C p.S677T 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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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries