Variant #0001164028 (NC_000012.11:g.266266T>C, NM_001170738.1:c.2229T>C (IQSEC3))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.266266T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID IQSEC3_000080
Frequency 779/13000
Freq. EA 73/8596
Freq. AA 706/4404
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 16:39:18 +02:00 (CEST)
Date last edited 2014-04-28 02:55:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
IQSEC3 NM_001170738.1 ?/? c.2229T>C r.(=) p.(=)