Variant #0001686777 (NC_000019.9:g.1226471A>C, NM_000455.4:c.1127A>C (STK11))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.1226471A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID STK11_000076
Frequency 1/12362
Freq. EA 1/8318
Freq. AA 0/4044
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:45:39 +02:00 (CEST)
Date last edited 2013-05-05 21:46:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

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