Variant #0001686761 (NC_000019.9:g.1222936C>T, NC_000019.9(NM_000455.4):c.921-48C>T (STK11))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.1222936C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID STK11_000060
Frequency 5/11356
Freq. EA 0/7652
Freq. AA 5/3704
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 21:46:41 +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.921-48C>T r.(=) p.(=)