Table 3.
BCL-6 Gene Status
| Case number | BCL-6 mutations | IgVH somatic mutations (≥2 × 10−2 bp) | Bcl-6 protein | MUM1/IRF4 protein |
|---|---|---|---|---|
| 528/95 | WT | Ne | + | + |
| 560/98 | A446G, A468C, T716G, G810C | Yes | − | + |
| 4111/99 | WT | Yes | − | + |
| 4365/99 | WT | Yes | + | + |
| 2700/00 | G799A | Ne | − | − |
| 3898/00 | A581G | GL | Ne | Ne |
| 3900/00 | WT | Ne | Ne | − |
| 3906/00 | WT | GL | + | + |
| 5463/00 | WT | Ne | − | − |
| 28/01 | G590C, G629C | GL | + | − |
| 29/01 | A581C | Yes | − | + |
| 33/01 | C742T | Ne | − | + |
| 35/01 | G759C | GL | − | + |
| 41/01 | WT | Yes | − | + |
| 47/01 | A436C, G478C, G481A, T495A, G518C, G533A | Ne | + | + |
| 64/01 | G518C, C525A, T548A, A551T, C601A, T633C | Ne | − | + |
| 65/01 | G478A, G533C, G540A, A541C, A547T, T554C, G578A, etc | Ne | + | − |
| 66/01 | G790T | Yes | + | − |
| 862/01 | T482C, T554G, C584G, G758C | GL | − | − |
| 838/01 | G708A, G810A | Ne | + | + |
| 857/01 | InsG706, C763T | GL | + | + |
| 866/01 | G485A | Ne | − | + |
| 867/01 | C584T, C765T | GL | − | + |
| 870/01 | T447C, T469A, C479T, G533A, A535C, A551C | Ne | + | + |
| 871/01 | G790A, T814C, T620A | Ne | + | − |
| 874/01 | C444G, G578C, T531C, C572G | Ne | + | + |
| 875/01 | G503A, G641A, C750T, insC770, T838G | Ne | − | + |
| 2837/00 | WT | Yes | − | − |
| 2838/00 | WT | Ne | Ne | Ne |
| 2839/00 | T466C, G804C | Yes | − | + |
| 2840/00 | G766T, C769G, C777T | Ne | + | + |
| 2841/00 | WT | Ne | Ne | Ne |
| 2842/00 | C744A, T739A, G833C | GL | − | + |
| 2843/00 | G488A, A535G, G549A, A551C, T557C, A582G, G621T;* | Ne | + | + |
| 2844/00 | T545G, A561C, C588T, G829A | Ne | − | Ne |
| 3409/00 | WT | Ne | − | Ne |
| 3903/00 | C704T | Ne | Ne | Ne |
Abbreviations: WT, wild type; *, mutation in homozygosis; GL, germline; Yes, presence of IgVH mutations (≥ 2 × 10−2 bp); +, positive result at immunohistochemistry; −, negativity at immunohistochemistry; Ne, not evaluable.