Variant #0000000067 (NC_000019.9:g.1226471A>C, NM_000455.4:c.1127A>C (STK11))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.1226471A>C
Reference -
DB-ID STK11_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2019-02-21 11:00:01 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STK11 NM_000455.4 ?/? 9 c.1127A>C r.(?) p.(Glu376Ala)