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Gene | MSH6 |
Variant | E1322* |
Impact List | nonsense |
Protein Effect | unknown |
Gene Variant Descriptions | MSH6 E1322* results in a premature truncation of the Msh6 protein at amino acid 1322 of 1360 (UniProt.org). E1322* has been identified in the scientific literature (PMID: 36765365, PMID: 31175329, PMID: 24755471), 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 E1322* |
Transcript | NM_000179.3 |
gDNA | chr2:g.47806614G>T |
cDNA | c.3964G>T |
Protein | p.E1322* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000179 | chr2:g.47806614G>T | c.3964G>T | p.E1322* | RefSeq | GRCh38/hg38 |
NM_001406804.1 | chr2:g.47806819G>T | c.3964G>T | p.E1322* | RefSeq | GRCh38/hg38 |
NM_001406809.1 | chr2:g.47806614G>T | c.3964G>T | p.E1322* | RefSeq | GRCh38/hg38 |
NM_001406796.1 | chr2:g.47806614G>T | c.3964G>T | p.E1322* | RefSeq | GRCh38/hg38 |
NM_000179.3 | chr2:g.47806614G>T | c.3964G>T | p.E1322* | RefSeq | GRCh38/hg38 |
NM_000179.2 | chr2:g.47806614G>T | c.3964G>T | p.E1322* | RefSeq | GRCh38/hg38 |
NM_001406808.1 | chr2:g.47806614G>T | c.3964G>T | p.E1322* | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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