Variant #0001065085 (NC_000011.9:g.9025388G>T, NM_020645.2:c.95C>A (NRIP3))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.9025388G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NRIP3_000056
Frequency 1/12730
Freq. EA 0/8446
Freq. AA 1/4284
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 21:51:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NRIP3 NM_020645.2 ?/? c.95C>A r.(?) p.(Ala32Glu)