Variant #0001191096 (NC_000012.11:g.40012448A>T, NC_000012.11(NM_005164.3):c.939+31T>A (ABCD2))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.40012448A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCD2_000041
Frequency 5/13004
Freq. EA 0/8598
Freq. AA 5/4406
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 05:22:26 +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.939+31T>A r.(=) p.(=)