Variant #0000007586 (NC_000004.11:-, KIT(NM_000222.2):c.1676T>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_00006 See all 6 reported entries
Frequency 2/a family
Variant remarks The point mutation (VaP59~Ala) iden-

tified in our study is possibly a novel type of gain-of-

function mutation of c-kit, one that causes multiple

GISTs as well as cutaneous hyperpigmentation.
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 ./. 11 c.1676T>C - p.Val559Ala