Variant #0001117101 (NC_000011.9:g.67250676G>A, NM_003977.2:c.47G>A (AIP))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.67250676G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AIP_000005
Frequency 33/12990
Freq. EA 30/8590
Freq. AA 3/4400
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 16:37:25 +02:00 (CEST)
Date last edited 2014-02-05 14:39:47 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AIP NM_003977.2 ?/? c.47G>A r.(?) p.(Arg16His)