Variant #0001033273 (NC_000010.10:g.123278372C>T, NC_000010.10(NM_000141.4):c.939+1121G>A (FGFR2))

Chromosome 10
DNA change (genomic) (Relative to hg19 / GRCh37) g.123278372C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FGFR2_000127
Frequency 1/12344
Freq. EA 1/8340
Freq. AA 0/4004
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 20:48:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FGFR2 NM_000141.4 ?/? c.939+1121G>A r.(=) p.(=)