Variant #0001065079 (NC_000011.9:g.9009805G>A, NM_020645.2:c.199C>T (NRIP3))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.9009805G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NRIP3_000050
Frequency 7/12994
Freq. EA 5/8592
Freq. AA 2/4402
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 16:37:25 +02:00 (CEST)
Date last edited 2013-05-04 21:50:59 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NRIP3 NM_020645.2 ?/? c.199C>T r.(?) p.(Arg67Cys)