Variant #0001654266 (NC_000018.9:g.5416221C>T, NM_012307.2:c.1663G>A (EPB41L3))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.5416221C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID EPB41L3_000144
Frequency 739/13006
Freq. EA 269/8600
Freq. AA 470/4406
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 16:45:07 +02:00 (CEST)
Date last edited 2013-05-05 20:19:47 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
EPB41L3 NM_012307.2 ?/? c.1663G>A r.(?) p.(Ala555Thr)