Variant #0001283588 (NC_000013.10:g.48985552C>T, NC_000013.10(NM_000321.2):c.1695+29973C>T (RB1))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.48985552C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RB1_000084
Frequency 1/13006
Freq. EA 1/8600
Freq. AA 0/4406
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 05:53:48 +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.1695+29973C>T r.(=) p.(=)
LPAR6 NM_005767.5 ?/? c.1008G>A r.(=) p.(=)