Variant #0000014628 (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 3256C>G
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID STK11_00236
Frequency -
Variant remarks This nucleotide substitution cause s a premature stop codon, Tyr246X, presumablyresulting in a truncated protein.
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 ./. 06 c.? - ?