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Gene APC
Variant H1490fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions APC H1490fs results in a change in the amino acid sequence of the Apc protein beginning at aa 1490 of 2843, likely resulting in premature truncation of the functional protein (UniProt.org). H1490fs has not been characterized, however, due to the effects of other truncation mutations downstream of H1490 (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 H1490fs

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Transcript NM_000038.6
gDNA chr5:g.(112840061_112840062)
cDNA c.(4468_4467)
Protein p.H1490fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001127510.3 chr5:g.(112840061_112840062) c.(4468_4467) p.H1490fs RefSeq GRCh38/hg38
NM_001127510.2 chr5:g.(112840061_112840062) c.(4468_4467) p.H1490fs RefSeq GRCh38/hg38
NM_001407450.1 chr5:g.(112840061_112840062) c.(4468_4467) p.H1490fs RefSeq GRCh38/hg38
NM_000038.6 chr5:g.(112840061_112840062) c.(4468_4467) p.H1490fs RefSeq GRCh38/hg38
NM_000038 chr5:g.(112840061_112840062) c.(4468_4467) p.H1490fs RefSeq GRCh38/hg38
NM_001127510 chr5:g.(112840061_112840062) c.(4468_4467) p.H1490fs RefSeq GRCh38/hg38
NM_000038.5 chr5:g.(112840061_112840062) c.(4468_4467) p.H1490fs RefSeq GRCh38/hg38
NM_001354895.1 chr5:g.(112840061_112840062) c.(4468_4467) p.H1490fs RefSeq GRCh38/hg38
NM_001354895.2 chr5:g.(112840061_112840062) c.(4468_4467) p.H1490fs RefSeq GRCh38/hg38

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  • 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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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries