Variant #0001993794 (NC_000023.10:g.153005532T>C, NC_000023.10(NM_000033.3):c.1489-14T>C (ABCD1))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.153005532T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCD1_000072
Frequency 2/10561
Freq. EA 0/6726
Freq. AA 2/3835
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 06:57:14 +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.1489-14T>C r.(=) p.(=)