Variant #0001993760 (NC_000023.10:g.152991616C>T, NM_000033.3:c.895C>T (ABCD1))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.152991616C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCD1_000063
Frequency 4/10100
Freq. EA 0/6469
Freq. AA 4/3631
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 16:50:35 +02:00 (CEST)
Date last edited 2018-08-23 11:15:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCD1 NM_000033.3 ?/? c.895C>T r.(?) p.(His299Tyr)