Variant #0001635203 (NC_000017.10:g.74465904T>C, NM_001088.2:c.476T>C (AANAT))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.74465904T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AANAT_000054
Frequency 1/12982
Freq. EA 1/8584
Freq. AA 0/4398
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 11:41:54 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AANAT NM_001088.2 ?/? c.476T>C r.(?) p.(Met159Thr)