Variant #0001519245 (NC_000016.9:g.83984756A>C, NC_000016.9(NM_182981.2):c.-2252A>C (OSGIN1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.83984756A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OSGIN1_000020
Frequency 421/11628
Freq. EA 2/7732
Freq. AA 419/3896
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 14:50:53 +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.-2252A>C r.(=) p.(=)