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Gene | APC |
Variant | C1578fs |
Impact List | frameshift |
Protein Effect | unknown |
Gene Variant Descriptions | APC C1578fs results in a change in the amino acid sequence of the Apc protein beginning at aa 1578 of 2843, likely resulting in premature truncation of the functional protein (UniProt.org). C1578fs has been identified in sequencing studies (PMID: 20102718), but has not been biochemically characterized and therefore, its effect on Apc protein function is unknown (PubMed, Aug 2024). |
Associated Drug Resistance | |
Category Variants Paths |
APC mutant APC C1578fs |
Transcript | NM_000038.6 |
gDNA | chr5:g.(112840325_112840326) |
cDNA | c.(4732_4731) |
Protein | p.C1578fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001354895.1 | chr5:g.(112840325_112840326) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_000038.6 | chr5:g.(112840325_112840326) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_001407472.1 | chr5:g.(112841477_112841478) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_000038.5 | chr5:g.(112840325_112840326) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_001407471.1 | chr5:g.(112841477_112841478) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_000038 | chr5:g.(112840325_112840326) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_001354895.2 | chr5:g.(112840325_112840326) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_001407450.1 | chr5:g.(112840325_112840326) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_001127510 | chr5:g.(112840325_112840326) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_001127510.2 | chr5:g.(112840325_112840326) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
NM_001127510.3 | chr5:g.(112840325_112840326) | c.(4732_4731) | p.C1578fs | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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