Variant #0000045624 (NC_000001.10:g.29508113T>C, NC_000001.10(NM_005626.4):c.107+45A>G (SRSF4))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.29508113T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SRSF4_000076
Frequency 2/12998
Freq. EA 0/8594
Freq. AA 2/4404
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 17:58:26 +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.107+45A>G r.(=) p.(=)