Variant #0000910831 (NC_000009.11:g.92011787A>G, NC_000009.11(NM_006378.3):c.316-37T>C (SEMA4D))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.92011787A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SEMA4D_000172
Frequency 219/13004
Freq. EA 3/8598
Freq. AA 216/4406
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 16:29:58 +02:00 (CEST)
Date last edited 2013-05-04 16:57:53 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SEMA4D NM_006378.3 ?/? c.316-37T>C r.(=) p.(=)