Variant #0004107730 (NC_000006.11:g.304655T>G, NM_020185.3:c.49T>G (DUSP22))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.304655T>G
DB-ID -
dbSNP ID rs748265668
gnomAD frequency 1/246272
gnomAD homozygote count 0/123135
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.49T>G r.(?) p.(Phe17Val)