Variant #0001283523 (NC_000013.10:g.48934122_48934125del, NC_000013.10(NM_000321.2):c.608-31_608-28del (RB1))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.48934122_48934125del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RB1_000031
Frequency 31/12502
Freq. EA 15/8242
Freq. AA 16/4260
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 16:41:01 +02:00 (CEST)
Date last edited 2013-05-05 05:53:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 ?/? c.608-31_608-28del r.(=) p.(=)