Variant #0001567579 (NC_000017.10:g.19286133_19286134insC, NM_139033.2:c.2171_2172insC (MAPK7))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.19286133_19286134insC
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MAPK7_000099
Frequency 47/12518
Freq. EA 23/8254
Freq. AA 24/4264
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 05:04:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MAPK7 NM_139033.2 ?/? c.2171_2172insC r.(?) p.(Leu726Profs*21)