Variant #0001033355 (NC_000010.10:g.123343236G>A, NC_000010.10(NM_000141.4):c.109+9987C>T (FGFR2))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.123343236G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FGFR2_000209
Frequency 164/4566
Freq. EA 1/3182
Freq. AA 163/1384
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 16:30:47 +02:00 (CEST)
Date last edited 2013-05-04 20:48:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FGFR2 NM_000141.4 ?/? c.109+9987C>T r.(=) p.(=)