Variant #0000833636 (NC_000008.10:g.38280709G>A, NC_000008.10(NM_001174063.1):c.937-1250C>T (FGFR1))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.38280709G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FGFR1_000095
Frequency 1/5734
Freq. EA 0/3982
Freq. AA 1/1752
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 16:29:29 +02:00 (CEST)
Date last edited 2013-05-04 14:42:33 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FGFR1 NM_001174063.1 ?/? c.937-1250C>T r.(=) p.(=)