Variant #0001932506 (NC_000022.10:g.41349520A>T, NC_000022.10(NM_014248.3):c.79-39A>T (RBX1))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.41349520A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RBX1_000009
Frequency 2/13006
Freq. EA 2/8600
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 16:50:05 +02:00 (CEST)
Date last edited 2013-05-06 08:26:24 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RBX1 NM_014248.3 ?/? c.79-39A>T r.(=) p.(=)