Variant #0001065069 (NC_000011.9:g.9009650T>C, NC_000011.9(NM_020645.2):c.339+15A>G (NRIP3))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.9009650T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NRIP3_000040
Frequency 1/12994
Freq. EA 1/8592
Freq. AA 0/4402
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 21:50:58 +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.339+15A>G r.(=) p.(=)