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Gene | APC |
Variant | S1215* |
Impact List | nonsense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | APC S1215* results in a premature truncation of the Apc protein at amino acid 1215 of 2843 (UniProt.org). S1215* has not been characterized, however, due to the effects of other truncation mutations downstream of S1215 (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 S1215* |
Transcript | NM_000038.6 |
gDNA | chr5:g.112839237_112839239delAGTinsTGA |
cDNA | c.3643_3645delAGTinsTGA |
Protein | p.S1215* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001354898.1 | chr5:g.112839312_112839314delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001354904.2 | chr5:g.112839615_112839617delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_000038.6 | chr5:g.112839237_112839239delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_000038 | chr5:g.112839237_112839239delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407469.1 | chr5:g.112839625C>A | c.3644C>A | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001127510.2 | chr5:g.112839237_112839239delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407456.1 | chr5:g.112839487_112839488delCTinsAA | c.3644_3645delCTinsAA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407451.1 | chr5:g.112839259C>A | c.3644C>A | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407472.1 | chr5:g.112840390C>A | c.3644C>A | p.S1215* | RefSeq | GRCh38/hg38 |
NM_000038.5 | chr5:g.112839237_112839239delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001127510.3 | chr5:g.112839237_112839239delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407455.1 | chr5:g.112839487_112839488delCTinsAA | c.3644_3645delCTinsAA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001354898.2 | chr5:g.112839312_112839314delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407471.1 | chr5:g.112840390C>A | c.3644C>A | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001354895.2 | chr5:g.112839237_112839239delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407454.1 | chr5:g.112839487_112839488delCTinsAA | c.3644_3645delCTinsAA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001354897.1 | chr5:g.112839207_112839209delAGCinsTGA | c.3643_3645delAGCinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407450.1 | chr5:g.112839237_112839239delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407467.1 | chr5:g.112839625C>A | c.3644C>A | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001354904.1 | chr5:g.112839615_112839617delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001354895.1 | chr5:g.112839237_112839239delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001354897.2 | chr5:g.112839207_112839209delAGCinsTGA | c.3643_3645delAGCinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001407457.1 | chr5:g.112839487_112839488delCTinsAA | c.3644_3645delCTinsAA | p.S1215* | RefSeq | GRCh38/hg38 |
NM_001127510 | chr5:g.112839237_112839239delAGTinsTGA | c.3643_3645delAGTinsTGA | p.S1215* | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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