Variant #0001283540 (NC_000013.10:g.48941595T>C, NC_000013.10(NM_000321.2):c.940-35T>C (RB1))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.48941595T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RB1_000049
Frequency 6/12964
Freq. EA 5/8572
Freq. AA 1/4392
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 05:53:46 +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.940-35T>C r.(=) p.(=)