Variant #0000007675 (NC_000004.11:-, KIT(NM_000222.2):c.1862C>A)

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_00064
Frequency -
Variant remarks We detected a nucleotide transversion of C1862A which results in Ala621Asp substitution in KIT protein in patient 1
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.1862C>A - p.Ala621Asp