Table 4.
AKT1 | APC | ATM | BRCA2 | cKIT | cMET | CTNNB1 | EGFR | ERBB4 | JAK3 | KDR | TP53 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
# positive | 1 | 1 | 1 | 1 | 1 | 1 | 9 | 1 | 1 | 1 | 1 | 13 |
Total tested | 28 | 29 | 28 | 6 | 34 | 29 | 28 | 31 | 29 | 28 | 28 | 28 |
% total | 3.6 | 3.4 | 3.6 | 16.7 | 2.9 | 3.4 | 32.1 | 3.2 | 3.4 | 3.6 | 3.6 | 46.4 |
Notes: Gene alterations were considered to be pathogenic or presumed pathogenic. Mutations of unknown significance, or believed to be benign (synonymous or missense), based on the ACCMG descriptions, were not reported. The test is not designed to distinguish somatic versus germline origin of the alteration. Genes tested for which no alterations were identified included ABL1, ALK, BRAF, BRCA1, CDH1, CSF1R, ERBB2, FBXW7, FGFR1, FGFR2, FLT3, GNA11, GNAQ, GNAS, HNF1A, HRAS, IDH1, JAK2, KRAS, MLH1, MPL, NOTCH1, NPM1, NRAS, PDGFRA, PIK3CA, PTEN, PTPN11, RB1, RET, SMAD4, SMARCB1, SMO, STK11, and VHL.