Variant #0000833677 (NC_000008.10:g.38287178A>C, NC_000008.10(NM_001174063.1):c.358+22T>G (FGFR1))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.38287178A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FGFR1_000136
Frequency 1/12910
Freq. EA 0/8540
Freq. AA 1/4370
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 14:42:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FGFR1 NM_001174063.1 ?/? c.358+22T>G r.(=) p.(=)