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| Gene | MSH6 |
| Variant | G1139S |
| Impact List | missense |
| Protein Effect | loss of function |
| Gene Variant Descriptions | MSH6 G1139S lies within the ATPase domain of the Msh6 protein (PMID: 17531815). G1139S (corresponds to G1137S in mouse) results in subcellular localization similar to wild-type Msh6 in culture (PMID: 22851212), but confers a loss of function to the Msh6 protein as indicated by reduced mismatch binding and impaired ATP binding (PMID: 31965077), defective mismatch repair activity in in vitro assays (PMID: 22102614, PMID: 31965077), elevated microsatellite instability, and impaired DNA damage response in mouse cells (PMID: 24040339). |
| Associated Drug Resistance | |
| Category Variants Paths |
MSH6 mutant MSH6 inact mut MSH6 G1139S |
| Transcript | NM_000179.3 |
| gDNA | chr2:g.47803662G>A |
| cDNA | c.3415G>A |
| Protein | p.G1139S |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001406800.1 | chr2:g.47803662G>A | c.3415G>A | p.G1139S | RefSeq | GRCh38/hg38 |
| NM_001406809.1 | chr2:g.47803662G>A | c.3415G>A | p.G1139S | RefSeq | GRCh38/hg38 |
| NM_000179.3 | chr2:g.47803662G>A | c.3415G>A | p.G1139S | RefSeq | GRCh38/hg38 |
| NM_000179.2 | chr2:g.47803662G>A | c.3415G>A | p.G1139S | RefSeq | GRCh38/hg38 |
| NM_001406796.1 | chr2:g.47803662G>A | c.3415G>A | p.G1139S | RefSeq | GRCh38/hg38 |
| NM_000179 | chr2:g.47803662G>A | c.3415G>A | p.G1139S | RefSeq | GRCh38/hg38 |
| XM_024452819.1 | chr2:g.47803662G>A | c.3415G>A | p.G1139S | RefSeq | GRCh38/hg38 |
| NM_001406808.1 | chr2:g.47803662G>A | c.3415G>A | p.G1139S | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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