| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | BCL6, LOC100131635 (A517I) | Indel (missense variant +1 more) | not specified | |
| | BCL6, LOC100131635 (A493T) | Single nucleotide variant (missense variant) | not specified | |
| | BCL6, LOC100131635 (R459C) | Single nucleotide variant (missense variant) | not specified | |
| | LOC100131635, BCL6 (T455M) | Single nucleotide variant (missense variant) | not specified | |
| | BCL6, LOC100131635 (N389S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC100131635, BCL6 (A321V) | Single nucleotide variant (missense variant) | not specified | |
| | BCL6, LOC100131635 (E302G) | Single nucleotide variant (missense variant) | not specified | |
| | BCL6, LOC100131635 (E164D) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
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