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Gene | APC |
Variant | N1455Ifs*18 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | APC N1455Ifs*18 indicates a shift in the reading frame starting at amino acid 1455 and terminating 18 residues downstream causing a premature truncation of the 2843 amino acid Apc protein (UniProt.org). N1455Ifs*18 has not been characterized, however, due to the effects of other truncation mutations downstream of N1455 (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 N1455fs APC N1455Ifs*18 |
Transcript | NM_000038.6 |
gDNA | chr5:g.112839958delA |
cDNA | c.4364delA |
Protein | p.N1455Ifs*18 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001127510 | chr5:g.112839953delT | c.4359delT | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001127511.3 | chr5:g.112840011_112840012insTCCCCCCCCCAAA | c.4363_4364insTCCCCCCCCCAAA | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_000038 | chr5:g.112839953delT | c.4359delT | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001127511 | chr5:g.112840011_112840012insTCCCCCCCCCCTT | c.4363_4364insTCCCCCCCCCCTT | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001127510.3 | chr5:g.112839958delA | c.4364delA | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001354902.1 | chr5:g.(112840230_112840286) | c.(4363_4419) | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001354895.1 | chr5:g.112839958delA | c.4364delA | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001127510.2 | chr5:g.112839958delA | c.4364delA | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_000038.5 | chr5:g.112839958delA | c.4364delA | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001407450.1 | chr5:g.112839958delA | c.4364delA | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_000038.6 | chr5:g.112839958delA | c.4364delA | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001354902.2 | chr5:g.(112840230_112840286) | c.(4363_4419) | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001354895.2 | chr5:g.112839958delA | c.4364delA | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
NM_001127511.2 | chr5:g.112840011_112840012insTCCCCCCCCCAAA | c.4363_4364insTCCCCCCCCCAAA | p.N1455Ifs*18 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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