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Gene MSH6
Variant D667V
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MSH6 D667V lies within the connector domain of the Msh6 protein (PMID: 17531815). D667V has not been characterized and therefore, its effect on Msh6 protein function is unknown (PubMed, Apr 2024).
Associated Drug Resistance
Category Variants Paths

MSH6 mutant MSH6 D667V

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Transcript NM_000179.3
gDNA chr2:g.47799983A>T
cDNA c.2000A>T
Protein p.D667V
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001406796.1 chr2:g.47799983A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_001281492.1 chr2:g.47800373A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_000179.2 chr2:g.47799983A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
XM_024452819.1 chr2:g.47799983A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_000179.3 chr2:g.47799983A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_001406803.1 chr2:g.47799983A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_001406809.1 chr2:g.47799983A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_001281492.2 chr2:g.47800373A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_001281492 chr2:g.47800373A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_000179 chr2:g.47799983A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_001406808.1 chr2:g.47799983A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_001406798.1 chr2:g.47799983A>T c.2000A>T p.D667V RefSeq GRCh38/hg38
NM_001406800.1 chr2:g.47799983A>T c.2000A>T p.D667V 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 )
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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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  • Click on any column header arrows to sort by that column
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References