Variant #0001446350 (NC_000016.9:g.1779556C>T, NM_001040439.1:c.579C>T (MAPK8IP3))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.1779556C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MAPK8IP3_000042
Frequency 24/12272
Freq. EA 19/8304
Freq. AA 5/3968
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 16:42:42 +02:00 (CEST)
Date last edited 2013-05-05 11:58:00 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MAPK8IP3 NM_001040439.1 ?/? c.579C>T r.(=) p.(=)