Variant #0001446372 (NC_000016.9:g.1793494G>A, NC_000016.9(NM_001040439.1):c.744+17G>A (MAPK8IP3))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.1793494G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MAPK8IP3_000064
Frequency 3/12536
Freq. EA 2/8396
Freq. AA 1/4140
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 11:58:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MAPK8IP3 NM_001040439.1 ?/? c.744+17G>A r.(=) p.(=)