Variant #0000000761 (NC_000019.10:g.1223126C>G, NM_000455.4:c.1062C>G (STK11))

Individual ID 00000149
Chromosome 19
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.1223126C>G
Published as 1223125C>G
Reference Nurul-Syakima Ab Mutalib et al. (2014)dbSNP
DB-ID STK11_000001
dbSNP ID rs59912467
Frequency 2/9
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-11-10 14:59:08 +08:00 (CST)
Date last edited 2021-08-23 09:55:55 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
STK11 NM_000455.4 ./. - c.1062C>G - r.(?) p.(Phe354Leu) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000164 DNA PCR STK11 1 Nuur Athirah Binti Mohd Daud