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Gene APC
Variant E763*
Impact List nonsense
Protein Effect loss of function - predicted
Gene Variant Descriptions APC E763* results in a premature truncation of the Apc protein at amino acid 763 of 2843 (UniProt.org). E763* has not been characterized, however, due to the effects of other truncation mutations downstream of E763 (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 E763*

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Transcript NM_000038.6
gDNA chr5:g.112837881G>T
cDNA c.2287G>T
Protein p.E763*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001127510.2 chr5:g.112837881G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_001127510.3 chr5:g.112837881G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_001407467.1 chr5:g.112838268G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_001354895.1 chr5:g.112837881G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_001407450.1 chr5:g.112837881G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_000038 chr5:g.112837881G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_001407469.1 chr5:g.112838268G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_000038.5 chr5:g.112837881G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_000038.6 chr5:g.112837881G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_001127510 chr5:g.112837881G>T c.2287G>T p.E763* RefSeq GRCh38/hg38
NM_001354895.2 chr5:g.112837881G>T c.2287G>T p.E763* RefSeq GRCh38/hg38

Filtering

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  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References