Variant #0001283536 (NC_000013.10:g.48939015C>A, NC_000013.10(NM_000321.2):c.862-15C>A (RB1))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.48939015C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RB1_000045
Frequency 41/12430
Freq. EA 0/8212
Freq. AA 41/4218
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 2025-01-02 01:30:41 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RB1 NM_000321.2 ?/? c.862-15C>A r.(=) p.(=)