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Gene | MSH6 |
Variant | K1358fs |
Impact List | frameshift |
Protein Effect | unknown |
Gene Variant Descriptions | MSH6 K1358fs results in a change in the amino acid sequence of the Msh6 protein beginning at aa 1358 of 1360, likely resulting in premature truncation of the functional protein (UniProt.org). K1358fs has been identified in the scientific literature (PMID: 26436112, PMID: 34620004, PMID: 35958441), but has not been biochemically characterized and therefore, its effect on Msh6 protein function is unknown (PubMed, Apr 2024). |
Associated Drug Resistance | |
Category Variants Paths |
MSH6 mutant MSH6 K1358fs |
Transcript | NM_000179.3 |
gDNA | chr2:g.(47806848_47806849) |
cDNA | c.(4072_4071) |
Protein | p.K1358fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000179.2 | chr2:g.(47806848_47806849) | c.(4072_4071) | p.K1358fs | RefSeq | GRCh38/hg38 |
NM_000179.3 | chr2:g.(47806848_47806849) | c.(4072_4071) | p.K1358fs | RefSeq | GRCh38/hg38 |
NM_000179 | chr2:g.(47806848_47806849) | c.(4072_4071) | p.K1358fs | RefSeq | GRCh38/hg38 |
NM_001406809.1 | chr2:g.(47806848_47806849) | c.(4072_4071) | p.K1358fs | RefSeq | GRCh38/hg38 |
NM_001406796.1 | chr2:g.(47806848_47806849) | c.(4072_4071) | p.K1358fs | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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