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. 2023 Jul 10;19(2):65. doi: 10.3892/mco.2023.2661

Table I.

Short variants detected by DNA panel sequencing.

Gene Variant VAF OncoKB CGI COSMIC COSMIC_id ClinVar
CDK12 Arg271Lys 0.418   Passenger      
CDK6 Val62Gly 0.408   Driver      
HGF Asp330Val 0.416   Driver      
KDM5A Thr1343Ile 0.333   Passenger      
LRP1B Cys138Gly 0.613   Passenger      
MSH2 Met688Ile 0.611   Driver Pathogenic COSV 51886508 US
SNCAIP Glu87Lys 0.035   Passenger Pathogenic COSV 54401827  
TP53 Splice acceptor of intron 8 0.849   Driver      

Blank cells mean that the records do not exist in the database. VAF, variant allele fraction; OncoKB, Memorial Sloan Kettering's Precision Oncology Knowledge Base; CGI, Cancer Genome Interpreter; COSMIC, Catalogue of Somatic Mutations in Cancer; US, uncertain significance.