Variant #0001176082 (NC_000012.11:g.8987211T>C, NC_000012.11(NM_144670.4):c.463-47T>C (A2ML1))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.8987211T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A2ML1_000048
Frequency 1/11876
Freq. EA 1/8184
Freq. AA 0/3692
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 04:26:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A2ML1 NM_144670.4 ?/? c.463-47T>C r.(=) p.(=)