Variant #0001567557 (NC_000017.10:g.19285448C>T, NM_139033.2:c.1832C>T (MAPK7))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.19285448C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MAPK7_000077
Frequency 2/12980
Freq. EA 0/8584
Freq. AA 2/4396
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 16:44:12 +02:00 (CEST)
Date last edited 2021-09-07 04:58:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MAPK7 NM_139033.2 ?/? c.1832C>T r.(?) p.(Ala611Val)