Variant #0000363577 (NC_000003.11:g.41266013A>G, NC_000003.11(NM_001098210.1):c.14-4A>G (CTNNB1))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.41266013A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CTNNB1_000012
Frequency 129/13006
Freq. EA 2/8600
Freq. AA 127/4406
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 16:23:53 +02:00 (CEST)
Date last edited 2013-05-04 01:49:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CTNNB1 NM_001098210.1 ?/? c.14-4A>G r.spl? p.?