Variant #0000045617 (NC_000001.10:g.29486852C>T, NC_000001.10(NM_005626.4):c.250+35G>A (SRSF4))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.29486852C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SRSF4_000069
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 17:58:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SRSF4 NM_005626.4 ?/? c.250+35G>A r.(=) p.(=)