Variant #0000007582 (NC_000004.11:-, KIT(NM_000222.2):c.253delG)

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID KIT_00001
Frequency -
Variant remarks The codon 85 frameshift constitutes a pure loss of function mutation, demonstrating that human piebaldism can result from simple haplo-insufficiency for KIT-dependent signal transduction.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIT NM_000222.2 ./. 02 c.253delG - p.Glu85LysfsX16