Variant #0000862910 (NC_000008.10:g.125498268G>C, NM_007218.3:c.378G>C (RNF139))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.125498268G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RNF139_000023
Frequency 1/13006
Freq. EA 0/8600
Freq. AA 1/4406
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 15:35:02 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RNF139 NM_007218.3 ?/? c.378G>C r.(=) p.(=)