Table 2.

Intraclonal variation of lymphomaVH gene sequences

Case no. Sequences analyzed (no.)Noncommon mutations*
Total (no.)Frequency (%) Distribution
1  3  3  0.34 (1-2/3), (1-1/3) × 2  
2  4  3  0.26  (3-2/4) 
3  3  0  0  
4  3  5  0.67  (1-2/3), (1-1/3) × 4  
5  2  1  0.17  (1-1/2)  
6  1  0.11  (1-1/2)  
7  2  0  0  
8  not cloned 
9  4  1  0.09  (1-3/4)  
10  3  1  0.11 (1-1/3)  
11  3  0  0  
12  4  12  0.94 (4-3/4), (1-2/4), (1-1/4) × 7  
13  2  0  0  
14 5  9  0.61  (3-3/5), (4-2/5), (1-1/5) × 2 
Case no. Sequences analyzed (no.)Noncommon mutations*
Total (no.)Frequency (%) Distribution
1  3  3  0.34 (1-2/3), (1-1/3) × 2  
2  4  3  0.26  (3-2/4) 
3  3  0  0  
4  3  5  0.67  (1-2/3), (1-1/3) × 4  
5  2  1  0.17  (1-1/2)  
6  1  0.11  (1-1/2)  
7  2  0  0  
8  not cloned 
9  4  1  0.09  (1-3/4)  
10  3  1  0.11 (1-1/3)  
11  3  0  0  
12  4  12  0.94 (4-3/4), (1-2/4), (1-1/4) × 7  
13  2  0  0  
14 5  9  0.61  (3-3/5), (4-2/5), (1-1/5) × 2 
*

Noncommon mutations represent single nucleotide sequence differences identified in only a proportion of theVH clones analyzed. The column labeled “distribution” indicates the number ofVH sequences that contained the noncommon mutation, ie, (2-3/5) indicates that 2 of the noncommon mutations were identified in 3 of 5 VH clones analyzed. Noncommon mutations found in more than half of theVH clones were included in the consensus sequences.

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