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| Gene | APC |
| Variant | D1636Gfs*2 |
| Impact List | frameshift |
| Protein Effect | unknown |
| Gene Variant Descriptions | APC D1636Gfs*2 indicates a shift in the reading frame starting at amino acid 1636 and terminating two residues downstream causing a premature truncation of the 2843 amino acid Apc protein (UniProt.org). D1636Gfs*2 has been identified in sequencing studies (PMID: 36013219, PMID: 37232746), but has not been biochemically characterized and therefore, its effect on Apc protein function is unknown (PubMed, May 2026). |
| Associated Drug Resistance | |
| Category Variants Paths |
APC mutant APC D1636fs APC D1636Gfs*2 |
| Transcript | NM_000038.6 |
| gDNA | chr5:g.112840500dupG |
| cDNA | c.4906dupG |
| Protein | p.D1636Gfs*2 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001354895.1 | chr5:g.112840500dupG | c.4906dupG | p.D1636Gfs*2 | RefSeq | GRCh38/hg38 |
| NM_001127510.2 | chr5:g.112840500dupG | c.4906dupG | p.D1636Gfs*2 | RefSeq | GRCh38/hg38 |
| NM_000038.6 | chr5:g.112840500dupG | c.4906dupG | p.D1636Gfs*2 | RefSeq | GRCh38/hg38 |
| NM_000038.5 | chr5:g.112840500dupG | c.4906dupG | p.D1636Gfs*2 | RefSeq | GRCh38/hg38 |
| NM_001354895.2 | chr5:g.112840500dupG | c.4906dupG | p.D1636Gfs*2 | RefSeq | GRCh38/hg38 |
| NM_001127510.3 | chr5:g.112840500dupG | c.4906dupG | p.D1636Gfs*2 | RefSeq | GRCh38/hg38 |
| NM_001407450.1 | chr5:g.112840500dupG | c.4906dupG | p.D1636Gfs*2 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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