Variant #0000568764 (NC_000005.9:g.112102949C>T, NM_000038.5:c.284C>T (APC))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.112102949C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID APC_000017
Frequency 2/13004
Freq. EA 0/8600
Freq. AA 2/4404
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:26:58 +02:00 (CEST)
Date last edited 2017-01-14 05:30:30 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
APC NM_000038.5 ?/? c.284C>T r.(?) p.(Ser95Phe)