Variant #0001635190 (NC_000017.10:g.74465448T>A, NC_000017.10(NM_001088.2):c.318+39T>A (AANAT))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.74465448T>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AANAT_000041
Frequency 525/13004
Freq. EA 139/8598
Freq. AA 386/4406
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 16:44:12 +02:00 (CEST)
Date last edited 2018-08-23 00:36:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AANAT NM_001088.2 ?/? c.318+39T>A r.(=) p.(=)