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Gene | APC |
Variant | N1455fs |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | APC N1455fs results in a change in the amino acid sequence of the Apc protein beginning at aa 1455 of 2843, likely resulting in premature truncation of the functional protein (UniProt.org). N1455fs 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 |
Transcript | NM_000038.6 |
gDNA | chr5:g.(112839956_112839957) |
cDNA | c.(4363_4362) |
Protein | p.N1455fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001354895.1 | chr5:g.(112839956_112839957) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_000038.5 | chr5:g.(112839956_112839957) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001127510 | chr5:g.(112839956_112839957) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001354902.2 | chr5:g.(112840229_112840230) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001127510.3 | chr5:g.(112839956_112839957) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001127511 | chr5:g.(112840010_112840011) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001407450.1 | chr5:g.(112839956_112839957) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_000038 | chr5:g.(112839956_112839957) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001354902.1 | chr5:g.(112840229_112840230) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_000038.6 | chr5:g.(112839956_112839957) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001127511.2 | chr5:g.(112840010_112840011) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001354895.2 | chr5:g.(112839956_112839957) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001127510.2 | chr5:g.(112839956_112839957) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
NM_001127511.3 | chr5:g.(112840010_112840011) | c.(4363_4362) | p.N1455fs | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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