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- W4313377531 abstract "BRCA1 and BRCA2 are the most mutated genes in breast cancer. We analyzed 48 breast cancer subjects using two methods that differ in terms of number of genes investigated and strategy used (primers: Panel A - 12 genes - vs probes: Panel B - 48 genes). Both the panels and procedures identified “pathogenic” or “likely pathogenic” variants in TP53, ATM, CHEK2 and BARD1 besides BRCA1 and BRCA2. Panel B identified two other putatively pathogenic variants in RNASEL and in RAD50. Identification of variants other than the BRCA genes can be useful in patient management. A total of 121 variants were distributed within the 12 genes and were correctly detected by both panels. However, the number of calls without divergence, namely ± 0.10 difference of allelic frequency, was 78.3%, while calls with a divergence below 0.10 was 16.7%, thus indicating that only 5% (n = 275) of 5,412 calls had a divergence above 0.10. Although these panels differ from each other, both are useful in different situations, particularly when patients should be tested for genes other than BRCA1/2 (as occurs in patients affected by a so called hereditary syndrome) or for therapeutic purposes." @default.
- W4313377531 created "2023-01-06" @default.
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- W4313377531 date "2023-01-01" @default.
- W4313377531 modified "2023-10-14" @default.
- W4313377531 title "The performance of multi-gene panels for breast/ovarian cancer predisposition" @default.
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- W4313377531 doi "https://doi.org/10.1016/j.cca.2022.12.007" @default.
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