Variant #0001436467 (NC_000016.9:g.108408C>T, NM_022450.3:c.2499G>A (RHBDF1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.108408C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RHBDF1_000008
Frequency 1019/13006
Freq. EA 167/8600
Freq. AA 852/4406
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 16:42:42 +02:00 (CEST)
Date last edited 2014-06-16 09:53:14 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RHBDF1 NM_022450.3 ?/? c.2499G>A r.(=) p.(=)