Variant #0001273268 (NC_000013.10:g.28644779G>C, NC_000013.10(NM_004119.2):c.44-30C>G (FLT3))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.28644779G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FLT3_000213
Frequency 5/12992
Freq. EA 1/8588
Freq. AA 4/4404
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 16:41:01 +02:00 (CEST)
Date last edited 2013-05-05 05:31:59 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FLT3 NM_004119.2 ?/? c.44-30C>G r.(=) p.(=)