Variant #0001229724 (NC_000012.11:g.88899027G>T, NC_000012.11(NM_003994.5):c.699-15C>A (KITLG))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.88899027G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KITLG_000007
Frequency 1/13000
Freq. EA 0/8598
Freq. AA 1/4402
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 16:39:18 +02:00 (CEST)
Date last edited 2013-05-05 03:47:57 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KITLG NM_003994.5 ?/? c.699-15C>A r.(=) p.(=)