Variant #0000007607 (NC_000004.11:-, KIT(NM_000222.2):c.1621A>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_00018 See all 3 reported entries
Frequency -
Variant remarks This substitution may impair insertion of the KIT recepter into the cell membrane or may affect dimerization of the recepter polypeptide.
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 ./. 10 c.1621A>C - p.Met541Leu