Variant #0001910878 (NC_000022.10:g.24176287G>A, NC_000022.10(NM_003073.3):c.1119-41G>A (SMARCB1))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.24176287G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SMARCB1_000058
Frequency 1643/12912
Freq. EA 1098/8552
Freq. AA 545/4360
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 16:50:05 +02:00 (CEST)
Date last edited 2014-01-18 20:52:38 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SMARCB1 NM_003073.3 ?/? c.1119-41G>A r.(=) p.(=)