Variant #0001176763 (NC_000012.11:g.9260252A>G, NC_000012.11(NM_000014.4):c.759-12T>C (A2M))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.9260252A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A2M_000182
Frequency 8/12312
Freq. EA 0/8382
Freq. AA 8/3930
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 04:22:08 +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.759-12T>C r.(=) p.(=)