Variant #0000045598 (NC_000001.10:g.29475773T>C, NC_000001.10(NM_005626.4):c.669-35A>G (SRSF4))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.29475773T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SRSF4_000050
Frequency 1/12672
Freq. EA 0/8360
Freq. AA 1/4312
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 17:58:23 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SRSF4 NM_005626.4 ?/? c.669-35A>G r.(=) p.(=)