Variant #0000007620 (NC_000004.11:-, KIT(NM_000222.2):c.2T>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_00028
Frequency -
Variant remarks The second mutation was a novel change, 2T>C,

which affects the T of the ATG initiation codon

M1T and is likely to result in absence of translation

initiation
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 ./. 01 c.2T>C - p.Met1Thr