Variant #0001932504 (NC_000022.10:g.41347501T>C, NC_000022.10(NM_014248.3):c.78+21T>C (RBX1))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.41347501T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RBX1_000007
Frequency 2/13002
Freq. EA 0/8598
Freq. AA 2/4404
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RBX1 NM_014248.3 ?/? c.78+21T>C r.(=) p.(=)