Variant #0000007990 (NC_000019.10:g.1221276C>T, STK11(NM_000455.4):c.798C>T)

Individual ID 00001420
Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.1221276C>T
Reference -
DB-ID STK11_000014
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Silvina Sisterna-Hospital de Comunidad
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     

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DNA change (cDNA)     

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RNA change     

Review status     
STK11 NM_000455.4 ?/? 6 c.798C>T p.(=) Hetero no r.(=) -



Screenings


AscendingScreening ID     

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Variants found     

Owner     
0000001673 DNA CNV;SEQ-NG IACA Panel (ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53) 26-feb-2020 Multigenetic panel - 36 Silvina Sisterna-Hospital de Comunidad