Variant #0000007644 (NC_000004.11:-, KIT(NM_000222.2):c.1859T>C)

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID KIT_00037
Frequency -
Variant remarks the Val620Ala mutation is novel and may result in a previously undescribed phenotype

with melanocyte instability, leading to progressive loss of pigmentation as well as the progressive

appearance of the hyperpigmented macules
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIT NM_000222.2 ./. 12 c.1859T>C - p.Val620Ala