Variant #0001436478 (NC_000016.9:g.108661A>G, NM_022450.3:c.2246T>C (RHBDF1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.108661A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RHBDF1_000019
Frequency 1/13006
Freq. EA 0/8600
Freq. AA 1/4406
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 2014-05-03 20:30:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RHBDF1 NM_022450.3 ?/? c.2246T>C r.(?) p.(Phe749Ser)