Variant #0001654288 (NC_000018.9:g.5423563T>C, NC_000018.9(NM_012307.2):c.1164-11A>G (EPB41L3))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.5423563T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID EPB41L3_000166
Frequency 214/13006
Freq. EA 5/8600
Freq. AA 209/4406
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 20:19:53 +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.1164-11A>G r.(=) p.(=)