Variant #0000039005 (NC_000012.11:g.88939551T>C, NM_000899.4:c.107A>G (KITLG))

Chromosome 12
Allele Unknown
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.88939551T>C
DNA change (hg38) g.88545774T>C
Published as -
ISCN -
DB-ID KITLG_000002 See all 3 reported entries
Variant remarks expression cloning A375 human pigmented melanoma cells doubles melanin content (2.09)
Reference PubMed: Wang 2007
ClinVar ID -
dbSNP ID -
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 21:50:39 +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 +/. 2 c.107A>G r.(?) p.Asn36Ser


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