Variant #0001567511 (NC_000017.10:g.19284164T>C, NM_139033.2:c.642T>C (MAPK7))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.19284164T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MAPK7_000031
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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 2024-12-05 03:37:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MAPK7 NM_139033.2 ?/? c.642T>C r.(=) p.(=)