Variant #0000011744 (NC_000019.10:g.1223034C>T, STK11(NM_000455.5):c.970C>T)

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.1223034C>T
Reference -
DB-ID STK11_000027 See all 4 reported entries
dbSNP ID rs549474196
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Luisina Bruno-Instituto Fleming
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Protein     

Zygosity     

Co_ocurrence     

RNA change     

Review status     
STK11 NM_000455.5 ?/? 5 c.970C>T p.(Pro324Ser) Hetero no r.(?) -