Variant #0001556814 (NC_000017.10:g.9791184C>A, NC_000017.10(NM_004246.1):c.1285-65C>A (GLP2R))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.9791184C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID GLP2R_000099
Frequency 1/4566
Freq. EA 0/3182
Freq. AA 1/1384
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 2013-05-05 16:17:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
GLP2R NM_004246.1 ?/? c.1285-65C>A r.(=) p.(=)