Variant #0000039002 (NC_000012.11:g.89328335T>C, NM_000899.4:c.-354280A>G (KITLG))

Chromosome 12
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.89328335T>C
DNA change (hg38) g.88934558T>C
Published as -
ISCN -
DB-ID KITLG_000001 See all 3 reported entries
Variant remarks reduced LEF1 binding; KITLG expression 20% reduced in hair follicles; influences hair pigmentation, shift towards blond
Reference PubMed: Guenther 2014
ClinVar ID -
dbSNP ID rs12821256
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-07-21 20:05:25 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KITLG NM_000899.4 +/. _1 c.-354280A>G r.(=) p.(=)


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