Variant #0004107663 (NC_000006.11:g.292541T>C, NM_020185.3:c.2T>C (DUSP22))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.292541T>C
DB-ID -
dbSNP ID rs756655896
gnomAD frequency 1/234256
gnomAD homozygote count 0/117125
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
DUSP22 NM_020185.3 ./. c.2T>C r.(?) p.(Met1?)