Variant #0000862902 (NC_000008.10:g.125487568A>G, NC_000008.10(NM_007218.3):c.181+37A>G (RNF139))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.125487568A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RNF139_000015
Frequency 2/13006
Freq. EA 0/8600
Freq. AA 2/4406
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 16:29:29 +02:00 (CEST)
Date last edited 2013-05-04 15:35:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RNF139 NM_007218.3 ?/? c.181+37A>G r.(=) p.(=)