Variant #0001531380 (NC_000017.10:g.69443C>T, NM_006987.3:c.698G>A (RPH3AL))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.69443C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RPH3AL_000027
Frequency 2/13006
Freq. EA 1/8600
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 16:44:12 +02:00 (CEST)
Date last edited 2014-04-25 14:10:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RPH3AL NM_006987.3 ?/? c.698G>A r.(?) p.(Arg233Gln)