Variant #0001163972 (NC_000012.11:g.234962G>A, NM_001170738.1:c.787G>A (IQSEC3))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.234962G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID IQSEC3_000024
Frequency 52/8412
Freq. EA 50/5916
Freq. AA 2/2496
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 20:35:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
IQSEC3 NM_001170738.1 ?/? c.787G>A r.(?) p.(Gly263Ser)