Variant #0001392660 (NC_000015.9:g.48434477C>A, NM_016132.3:c.*628G>T (MYEF2))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.48434477C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MYEF2_000020
Frequency 1/12990
Freq. EA 0/8594
Freq. AA 1/4396
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 16:41:46 +02:00 (CEST)
Date last edited 2013-05-05 09:56:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MYEF2 NM_016132.3 ?/? c.*628G>T r.(?) p.(Leu478Ile)
SLC24A5 NM_205850.2 ?/? c.1432C>A r.(?) p.(Leu478Ile)