Variant #0001229718 (NC_000012.11:g.88898895_88898896insT, NC_000012.11(NM_003994.5):c.*37+40_*37+41insA (KITLG))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.88898895_88898896insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KITLG_000001
Frequency 4/12478
Freq. EA 3/8230
Freq. AA 1/4248
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 03:47:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KITLG NM_003994.5 ?/? c.*37+40_*37+41insA r.(=) p.(=)