pISSN 2234-3806eISSN 2234-3814
Table. 2.
Commonly detected mutations in our study
| Gene | Frequency | N by mutation type |
|---|---|---|
| 38.3% (31/81) | 31 SNVs and 4 indels | |
| 13.6% (11/81) | 5 SNVs and 6 indels | |
| 9.9% (8/81) | 8 SNVs | |
| 9.4% (3/32) | 1 SNV and 3 indels | |
| 4.9% (4/81) | 4 SNVs | |
| 3.7% (3/81) | 4 SNVs | |
| 6.2% (5/81) | 5 amplifications | |
| 4.9% (4/81) | 4 amplifications | |
| 9.4% (3/32) | 3 amplifications | |
| 9.4% (3/32) | 3 amplifications | |
| 3.7% (3/81) | 3 amplifications | |
| 3.7% (3/81) | 3 amplifications |
*CNVs were detected in these genes.
Abbreviations: SNV, single-nucleotide variant; CNV, copy number variation.
Ann Lab Med 2024;44:164~173 https://doi.org/10.3343/alm.2023.0187
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