Variant #0000014680 (NC_000019.9:-, STK11(NM_000455.4):c.-1114_290+1del)

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Exon 1 deleted
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID STK11_00462
Frequency -
Variant remarks male,Clinical presentation:Buccal freckling, polyps

male,Clinical presentation:Multiple polyps

female,Clinical presentation:Multiple polyps, buccal freckling
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     
STK11 NM_000455.4 ./. 01 c.-1114_290+1del - ?