Variant #0001163974 (NC_000012.11:g.235028G>A, NM_001170738.1:c.853G>A (IQSEC3))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.235028G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID IQSEC3_000026
Frequency 1/8446
Freq. EA 1/5976
Freq. AA 0/2470
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 2014-03-13 05:19:03 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
IQSEC3 NM_001170738.1 ?/? c.853G>A r.(?) p.(Ala285Thr)