Variant #0001163975 (NC_000012.11:g.235095_235096insG, NC_000012.11(NM_001170738.1):c.903+17_903+18insG (IQSEC3))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.235095_235096insG
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID IQSEC3_000027
Frequency 93/6738
Freq. EA 84/4722
Freq. AA 9/2016
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 03:00:40 +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.903+17_903+18insG r.(=) p.(=)