Table 2.
Genes harboring point mutations in greater than 5% of Black or White TNBC cases.
| % of TNBC cases | |||
|---|---|---|---|
| Gene symbol | Black N=71 | White N=62 | Pa |
| ADGRG4 | 5.6 | 1.6 | 0.37 |
| AFF2 | 5.6 | 3.2 | 0.68 |
| ARID1A | 5.6 | 3.2 | 0.68 |
| ARID2 | 5.6 | 1.6 | 0.37 |
| ATR | 4.2 | 6.5 | 0.70 |
| BRCA1 | 2.8 | 6.5 | 0.42 |
| COL6A3 | 7.0 | 8.1 | 1.00 |
| HMCN1 | 7.0 | 6.5 | 1.00 |
| KIF4A | 5.6 | 1.6 | 0.37 |
| KMT2A | 5.6 | 8.1 | 0.73 |
| KMT2C | 8.5 | 4.8 | 0.50 |
| KMT2D | 8.5 | 6.5 | 0.75 |
| MDN1 | 9.9 | 4.8 | 0.34 |
| NCOR1 | 1.4 | 9.7 | 0.05 |
| PIK3CA | 2.8 | 12.9 | 0.04 |
| RYR2 | 9.9 | 16.1 | 0.31 |
| SYNE1 | 14.1 | 6.5 | 0.17 |
| SYNE2 | 4.2 | 8.1 | 0.47 |
| TP53 | 63.4 | 75.8 | 0.13 |
| UBR5 | 7.0 | 4.8 | 0.72 |
| USH2A | 5.6 | 3.2 | 0.68 |
| USP9X | 5.6 | 1.6 | 0.37 |
a.
Fisher’s Exact Test