Variant #0000514454 (NC_000004.11:g.146046138T>C, NC_000004.11(NM_002940.2):c.1641-4T>C (ABCE1))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.146046138T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ABCE1_000078
Frequency 12792/12968
Freq. EA 8582/8584
Freq. AA 4210/4384
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 16:25:12 +02:00 (CEST)
Date last edited 2018-08-23 08:27:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCE1 NM_002940.2 ?/? c.1641-4T>C r.spl? p.?