Variant #0001176076 (NC_000012.11:g.8982393G>A, NC_000012.11(NM_144670.4):c.462+18G>A (A2ML1))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.8982393G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A2ML1_000041
Frequency 44/12468
Freq. EA 0/8380
Freq. AA 44/4088
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 2018-08-22 23:41:23 +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.462+18G>A r.(=) p.(=)