Variant #0001191060 (NC_000012.11:g.39979911A>T, NC_000012.11(NM_005164.3):c.1792+43T>A (ABCD2))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.39979911A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCD2_000018
Frequency 121/13004
Freq. EA 110/8598
Freq. AA 11/4406
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 12:58:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCD2 NM_005164.3 ?/? c.1792+43T>A r.(=) p.(=)