Variant #0001531386 (NC_000017.10:g.69544A>G, NC_000017.10(NM_006987.3):c.614-17T>C (RPH3AL))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.69544A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID RPH3AL_000033
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 16:44:12 +02:00 (CEST)
Date last edited 2014-04-24 12:46:17 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
RPH3AL NM_006987.3 ?/? c.614-17T>C r.(=) p.(=)