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Gene | MSH6 |
Variant | P1097S |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | MSH6 P1097S lies within the ATPase domain of the Msh6 protein (PMID: 17531815). P1097S has been identified in sequencing studies (PMID: 28002797, PMID: 35522273), but has not been biochemically characterized and therefore, its effect on Msh6 protein function is unknown (PubMed, Jun 2024). |
Associated Drug Resistance | |
Category Variants Paths |
MSH6 mutant MSH6 P1097S |
Transcript | NM_000179.3 |
gDNA | chr2:g.47803536C>T |
cDNA | c.3289C>T |
Protein | p.P1097S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001406796.1 | chr2:g.47803536C>T | c.3289C>T | p.P1097S | RefSeq | GRCh38/hg38 |
NM_000179 | chr2:g.47803536C>T | c.3289C>T | p.P1097S | RefSeq | GRCh38/hg38 |
XM_024452819.1 | chr2:g.47803536C>T | c.3289C>T | p.P1097S | RefSeq | GRCh38/hg38 |
NM_000179.3 | chr2:g.47803536C>T | c.3289C>T | p.P1097S | RefSeq | GRCh38/hg38 |
NM_001406808.1 | chr2:g.47803536C>T | c.3289C>T | p.P1097S | RefSeq | GRCh38/hg38 |
NM_001406809.1 | chr2:g.47803536C>T | c.3289C>T | p.P1097S | RefSeq | GRCh38/hg38 |
NM_001406800.1 | chr2:g.47803536C>T | c.3289C>T | p.P1097S | RefSeq | GRCh38/hg38 |
NM_000179.2 | chr2:g.47803536C>T | c.3289C>T | p.P1097S | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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