Variant #0001567558 (NC_000017.10:g.19285463C>T, NM_139033.2:c.1847C>T (MAPK7))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.19285463C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MAPK7_000078
Frequency 5/12988
Freq. EA 1/8590
Freq. AA 4/4398
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 16:44:12 +02:00 (CEST)
Date last edited 2021-09-07 05:13:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MAPK7 NM_139033.2 ?/? c.1847C>T r.(?) p.(Pro616Leu)