Variant #0000862888 (NC_000008.10:g.125487350C>T, NM_007218.3:c.-1C>T (RNF139))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.125487350C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RNF139_000001
Frequency 1/9616
Freq. EA 0/6564
Freq. AA 1/3052
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.-1C>T r.(=) p.(=)