Skip to main content
. Author manuscript; available in PMC: 2012 Mar 1.
Published in final edited form as: Mol Cancer Res. 2011 Feb 22;9(3):271–279. doi: 10.1158/1541-7786.MCR-10-0496

Table 2.

Relationship of clinical variables to functional classification of p53 germline alleles based on DN90. For each allele, the DN effect was determined quantitatively (luciferase-based) in 4 different reporter strains. Alleles were classified as DN or recessive (rec) if they reduced (or not) the transactivation activity of the WT allele to less than 90% (DN90), respectively, in at least one of the four reporter strains. The p values are for testing whether the proportion of families exhibiting a given clinical characteristic differed according to the type of allele carried by the family.

DN90 rec O-SD DN90
vs rec
(p value)
DN90
vs O-SD
(p value)
rec
vs O-SD
(p value)
Number of alleles 60 (58%) 43 (42%) 52
Class distribution of families
NA 7 (5%) 5 (8%) 2 (3%) ns ns ns
noFH 22 (14%) 9 (14%) 5 (7%) ns ns ns
FH 20 (13%) 19 (30%) 6 (9%) 0.006 ns 0.002
LFL 44 (29%) 14 (22%) 24 (34%) ns ns ns
LFS 59 (39%) 16 (25%) 33 (47%) ns ns 0.012
Total 152 (100%) 63 (100%) 70 (100%)
Families with individuals
exhibiting multiple tumours
96 (63%) 28 (44%) 40 (57%) 0.015 ns ns