Variant #0000780328 (NC_000007.13:g.117188682G>T, NC_000007.13(NM_000492.3):c.1210-13G>T (CFTR))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.117188682G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CFTR_000101
Frequency 1595/12976
Freq. EA 1146/8576
Freq. AA 449/4400
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 13:09:57 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CFTR NM_000492.3 ?/? c.1210-13G>T r.(=) p.(=)