Variant #0001450541 (NC_000016.9:g.2165630T>C, NC_000016.9(NM_000296.3):c.1850-4A>G (PKD1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2165630T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PKD1_000902
Frequency 2723/11952
Freq. EA 1196/8014
Freq. AA 1527/3938
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 16:42:42 +02:00 (CEST)
Date last edited 2013-05-05 12:07:05 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PKD1 NM_000296.3 ?/? c.1850-4A>G r.spl? p.?