Variant #0001176751 (NC_000012.11:g.9259076A>T, NC_000012.11(NM_000014.4):c.994+11T>A (A2M))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.9259076A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A2M_000170
Frequency 139/11904
Freq. EA 2/8176
Freq. AA 137/3728
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 00:57:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A2M NM_000014.4 ?/? c.994+11T>A r.(=) p.(=)