Variant #0001450569 (NC_000016.9:g.2168156C>T, NM_000296.3:c.837G>A (PKD1))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.2168156C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PKD1_000930
Frequency 2/11842
Freq. EA 2/8058
Freq. AA 0/3784
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 12:07:07 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PKD1 NM_000296.3 ?/? c.837G>A r.(=) p.(=)