Variant #0001283553 (NC_000013.10:g.48947576T>G, NM_000321.2:c.1163T>G (RB1))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.48947576T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RB1_000066
Frequency 1/12980
Freq. EA 1/8576
Freq. AA 0/4404
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 16:41:01 +02:00 (CEST)
Date last edited 2013-05-05 05:53:47 +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.1163T>G r.(?) p.(Ile388Ser)