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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 |
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_000179.2 | 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_001406798.1 | 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_001406796.1 | 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 |
NM_001281492 | chr2:g.47800373A>T | c.2000A>T | p.D667V | RefSeq | GRCh38/hg38 |
NM_001281492.2 | chr2:g.47800373A>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_001281492.1 | 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_001406809.1 | 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 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
MSH6 D667V | unknown |