Variant #0000780360 (NC_000007.13:g.117199709G>A, NM_000492.3:c.1584G>A (CFTR))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.117199709G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CFTR_000132
Frequency 187/13006
Freq. EA 159/8600
Freq. AA 28/4406
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 16:28:58 +02:00 (CEST)
Date last edited 2013-05-04 13:10:01 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CFTR NM_000492.3 ?/? c.1584G>A r.(=) p.(=)