Variant #0001273216 (NC_000013.10:g.28624192C>T, NC_000013.10(NM_004119.2):c.742+40G>A (FLT3))

Chromosome 13
DNA change (genomic) (Relative to hg19 / GRCh37) g.28624192C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FLT3_000161
Frequency 12/13006
Freq. EA 3/8600
Freq. AA 9/4406
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 2025-01-06 18:06:25 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FLT3 NM_004119.2 ?/? c.742+40G>A r.(=) p.(=)