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Gene APC
Variant Q1447*
Impact List nonsense
Protein Effect loss of function - predicted
Gene Variant Descriptions APC Q1447* results in a premature truncation of the Apc protein at aa 1447 of 2843 (UniProt.org). Q1447* has not been characterized, however, due to the effects of other truncation mutations downstream of Q1447 (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 Q1447*

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Transcript NM_000038.6
gDNA chr5:g.112839933C>T
cDNA c.4339C>T
Protein p.Q1447*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001407449.1 chr5:g.112839879C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001354895.1 chr5:g.112839933C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001407447.1 chr5:g.112839879C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001127510.2 chr5:g.112839933C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001354896.2 chr5:g.112839879C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001127510 chr5:g.112839933C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_000038.5 chr5:g.112839933C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001407450.1 chr5:g.112839933C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001354896.1 chr5:g.112839879C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001127510.3 chr5:g.112839933C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001407448.1 chr5:g.112839879C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_000038.6 chr5:g.112839933C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_000038 chr5:g.112839933C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38
NM_001354895.2 chr5:g.112839933C>T c.4339C>T p.Q1447* RefSeq GRCh38/hg38

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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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