Variant #0001273269 (NC_000013.10:g.28647534T>G, NC_000013.10(NM_004119.2):c.44-2785A>C (FLT3))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.28647534T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FLT3_000214
Frequency 187/5720
Freq. EA 2/3972
Freq. AA 185/1748
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 05:32:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FLT3 NM_004119.2 ?/? c.44-2785A>C r.(=) p.(=)