Variant #0000915850 (NC_000009.11:g.99404124G>C, NM_153698.1:c.598C>G (AAED1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.99404124G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAED1_000007
Frequency 6/13006
Freq. EA 5/8600
Freq. AA 1/4406
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 16:29:58 +02:00 (CEST)
Date last edited 2018-08-22 09:01:35 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAED1 NM_153698.1 ?/? c.598C>G r.(?) p.(His200Asp)