Variant #0000014480 (NC_000019.9:-, STK11(NM_000455.4):c.?)

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Exon 5 245 1-bp (C) deletion
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID STK11_00052
Frequency -
Variant remarks Frameshift; stop at codon 286
ClassClinical -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK11 NM_000455.4 ./. 05 c.? - p.?