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Gene | APC |
Variant | E1309Dfs*4 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | APC E1309Dfs*4 indicates a shift in the reading frame starting at amino acid 1309 and terminating 4 residues downstream causing a premature truncation of the 2843 amino acid Apc protein (UniProt.org). E1309Dfs*4 has not been characterized, however, based on the effects of a similar frameshift mutation at E1309 (PMID: 10213492, PMID: 17189293), is predicted to lead to a loss of Apc protein function. |
Associated Drug Resistance | |
Category Variants Paths |
APC mutant APC inact mut APC E1309fs APC E1309Dfs*4 |
Transcript | NM_000038.6 |
gDNA | chr5:g.112839520_112839521insCAACCCAT |
cDNA | c.3926_3927insCAACCCAT |
Protein | p.E1309Dfs*4 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000038.6 | chr5:g.112839520_112839521insCAACCCAT | c.3926_3927insCAACCCAT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_001407472.1 | chr5:g.112840672_112840673insCAACCCAT | c.3926_3927insCAACCCAT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_000038 | chr5:g.112839520_112839521insTTTCCCTT | c.3926_3927insTTTCCCTT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_001354895.2 | chr5:g.112839520_112839521insCAACCCAT | c.3926_3927insCAACCCAT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_001354895.1 | chr5:g.112839520_112839521insCAACCCAT | c.3926_3927insCAACCCAT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_001127510.3 | chr5:g.112839520_112839521insCAACCCAT | c.3926_3927insCAACCCAT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_001407471.1 | chr5:g.112840672_112840673insCAACCCAT | c.3926_3927insCAACCCAT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_000038.5 | chr5:g.112839520_112839521insCAACCCAT | c.3926_3927insCAACCCAT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_001127510 | chr5:g.112839520_112839521insTTTCCCTT | c.3926_3927insTTTCCCTT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_001407450.1 | chr5:g.112839520_112839521insCAACCCAT | c.3926_3927insCAACCCAT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
NM_001127510.2 | chr5:g.112839520_112839521insCAACCCAT | c.3926_3927insCAACCCAT | p.E1309Dfs*4 | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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