Variant #0000623490 (NC_000006.11:g.13642676A>T, NC_000006.11(NM_005493.2):c.1225+35T>A (RANBP9))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.13642676A>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RANBP9_000066
Frequency 172/13004
Freq. EA 2/8600
Freq. AA 170/4404
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 16:27:59 +02:00 (CEST)
Date last edited 2019-03-01 07:24:16 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RANBP9 NM_005493.2 ?/? c.1225+35T>A r.(=) p.(=)