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| Gene | APC |
| Variant | S1356* |
| Impact List | nonsense |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | APC S1356* results in a premature truncation of the Apc protein at amino acid 1356 of 2843 (UniProt.org). S1356* has not been characterized, however, due to the effects of other truncation mutations downstream of S1356 (PMID: 18199528, PMID: 10346819), is predicted to lead to a loss of Apc protein function. |
| Associated Drug Resistance | |
| Category Variants Paths |
APC mutant APC inact mut APC S1356* |
| Transcript | NM_000038.6 |
| gDNA | chr5:g.112839661C>A |
| cDNA | c.4067C>A |
| Protein | p.S1356* |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001407453.1 | chr5:g.112839837_112839839delAGTinsTGA | c.4066_4068delAGTinsTGA | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001127510 | chr5:g.112839661C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001354901.2 | chr5:g.112839837_112839839delAGTinsTGA | c.4066_4068delAGTinsTGA | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001354895.1 | chr5:g.112839661C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_000038.6 | chr5:g.112839661C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001354895.2 | chr5:g.112839661C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_000038 | chr5:g.112839661C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001407450.1 | chr5:g.112839661C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001127510.2 | chr5:g.112839661C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_000038.5 | chr5:g.112839661C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001127510.3 | chr5:g.112839661C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001354897.1 | chr5:g.112839631C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001354901.1 | chr5:g.112839837_112839839delAGTinsTGA | c.4066_4068delAGTinsTGA | p.S1356* | RefSeq | GRCh38/hg38 |
| NM_001354897.2 | chr5:g.112839631C>A | c.4067C>A | p.S1356* | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|---|---|---|---|---|---|---|
| APC S1356* | colorectal cancer | sensitive | G007-LK | Preclinical - Patient cell culture | Actionable | In a preclinical study, G007-LK inhibited viability of a patient-derived colorectal cancer cell line harboring APC S1356* in culture (PMID: 37968472). | 37968472 |