Variant #0000470827 (NC_000004.11:g.20520993T>C, NC_000004.11(NM_004787.1):c.1059-12T>C (SLIT2))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.20520993T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SLIT2_000077
Frequency 11404/12992
Freq. EA 7506/8590
Freq. AA 3898/4402
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 04:35:59 +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.1059-12T>C r.(=) p.(=)