Variant #0000000095 (NC_000005.10:g.112841553A>G, APC(NM_000038.5):c.5959A>G)

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.112841553A>G
Published as -
Reference N.A. Abdul Murad et al. (2012), dbSNP
DB-ID APC_000004
dbSNP ID rs1269798265
Frequency 76
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
APC NM_000038.5 ?/. 11i_15i c.5959A>G - r.(?) p.(Ile1987Val) - ClinVar