Variant #0001567547 (NC_000017.10:g.19285089C>T, NC_000017.10(NM_139033.2):c.1478-5C>T (MAPK7))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.19285089C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MAPK7_000067
Frequency 1/12938
Freq. EA 0/8558
Freq. AA 1/4380
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 2013-05-05 16:42:47 +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.1478-5C>T r.spl? p.?