Variant #0001519281 (NC_000016.9:g.83993043G>A, NC_000016.9(NM_182981.2):c.204+42G>A (OSGIN1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.83993043G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OSGIN1_000056
Frequency 1/12982
Freq. EA 0/8586
Freq. AA 1/4396
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 14:50:55 +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.204+42G>A r.(=) p.(=)