Variant #0001519262 (NC_000016.9:g.83991313A>C, NM_182981.2:c.37A>C (OSGIN1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.83991313A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OSGIN1_000037
Frequency 42/12982
Freq. EA 38/8590
Freq. AA 4/4392
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 16:42:42 +02:00 (CEST)
Date last edited 2013-05-05 14:50:54 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OSGIN1 NM_182981.2 ?/? c.37A>C r.(?) p.(Ser13Arg)