Variant #0001176123 (NC_000012.11:g.8991814G>A, NM_144670.4:c.1076G>A (A2ML1))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.8991814G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A2ML1_000093
Frequency 1/11944
Freq. EA 0/8202
Freq. AA 1/3742
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 2018-08-23 12:28:03 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A2ML1 NM_144670.4 ?/? c.1076G>A r.(?) p.(Gly359Glu)