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Gene | MSH6 |
Variant | A1320Sfs*5 |
Impact List | frameshift |
Protein Effect | unknown |
Gene Variant Descriptions | MSH6 A1320Sfs*5 indicates a shift in the reading frame starting at amino acid 1320 and terminating 5 residues downstream causing a premature truncation of the 1360 amino acid Msh6 protein (UniProt.org). A1320Sfs*5 has been identified in the scientific literature (PMID: 35739269, PMID: 33393477, PMID: 18809606), but has not been biochemically characterized and therefore, its effect on Msh6 protein function is unknown (PubMed, May 2024). |
Associated Drug Resistance | |
Category Variants Paths |
MSH6 mutant MSH6 A1320Sfs*5 |
Transcript | NM_000179.3 |
gDNA | chr2:g.47806607dupA |
cDNA | c.3957dupA |
Protein | p.A1320Sfs*5 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001406796.1 | chr2:g.47806607dupA | c.3957dupA | p.A1320Sfs*5 | RefSeq | GRCh38/hg38 |
NM_000179.3 | chr2:g.47806607dupA | c.3957dupA | p.A1320Sfs*5 | RefSeq | GRCh38/hg38 |
NM_001406809.1 | chr2:g.47806607dupA | c.3957dupA | p.A1320Sfs*5 | RefSeq | GRCh38/hg38 |
NM_001406808.1 | chr2:g.47806607dupA | c.3957dupA | p.A1320Sfs*5 | RefSeq | GRCh38/hg38 |
NM_000179.2 | chr2:g.47806607dupA | c.3957dupA | p.A1320Sfs*5 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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