Variant #0000470785 (NC_000004.11:g.20482380C>T, NM_004787.1:c.509C>T (SLIT2))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.20482380C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SLIT2_000043
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 16:25:12 +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.509C>T r.(?) p.(Ala170Val)