Variant #0000481070 (NC_000004.11:g.55569859_55569860insT, NC_000004.11(NM_000222.2):c.757-31_757-30insT (KIT))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.55569859_55569860insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KIT_000050
Frequency 46/12440
Freq. EA 26/8230
Freq. AA 20/4210
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 16:25:12 +02:00 (CEST)
Date last edited 2013-05-04 04:51:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KIT NM_000222.2 ?/? c.757-31_757-30insT r.(=) p.(=)