Variant #0000363582 (NC_000003.11:g.41266623T>C, NM_001098210.1:c.420T>C (CTNNB1))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.41266623T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CTNNB1_000017
Frequency 70/13006
Freq. EA 3/8600
Freq. AA 67/4406
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 2025-01-04 14:38:17 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CTNNB1 NM_001098210.1 ?/? c.420T>C r.(=) p.(=)