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Gene APC
Variant E1306fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions APC E1306fs results in a change in the amino acid sequence of the Apc protein beginning at aa 1306 of 2843, likely resulting in premature truncation of the functional protein (UniProt.org). E1306fs has not been characterized, however, due to the effects of other truncation mutations downstream of E1306 (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 E1306fs

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Transcript NM_000038.6
gDNA chr5:g.(112839509_112839510)
cDNA c.(3916_3915)
Protein p.E1306fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001127510 chr5:g.(112839509_112839510) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_000038 chr5:g.(112839509_112839510) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_001354895.2 chr5:g.(112839509_112839510) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_001127510.2 chr5:g.(112839509_112839510) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_001354902.2 chr5:g.(112839782_112839783) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_001407450.1 chr5:g.(112839509_112839510) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_001127510.3 chr5:g.(112839509_112839510) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_000038.6 chr5:g.(112839509_112839510) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_001354902.1 chr5:g.(112839782_112839783) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_000038.5 chr5:g.(112839509_112839510) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38
NM_001354895.1 chr5:g.(112839509_112839510) c.(3916_3915) p.E1306fs RefSeq GRCh38/hg38

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References