Variant #0000470793 (NC_000004.11:g.20487798_20487801del, NC_000004.11(NM_004787.1):c.540-25_540-22del (SLIT2))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.20487798_20487801del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SLIT2_000051
Frequency 72/12492
Freq. EA 10/8232
Freq. AA 62/4260
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 16:25:12 +02:00 (CEST)
Date last edited 2013-05-04 04:35:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SLIT2 NM_004787.1 ?/? c.540-25_540-22del r.(=) p.(=)