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. 2007 Jun;44(6):393–396. doi: 10.1136/jmg.2006.047530

Table 1 Mutations found in microdissected tumour samples.

Slides Tissue cell types CTNNB1 mutation Nucleotide change WT1 mutation* LOH analysis
Initial left tumour
A3 Tubuli S45P TCT>CCT m/m
A3 Stroma T41A ACC>GCC m/m
A3 Blastema S45P TCT>CCT m/m
A3 Stroma II S45P TCT>CCT nd
A3 Muscle I S45P TCT>CCT m/m
A3 Muscle II S45P TCT>CCT nd
A1 Muscle S45P TCT>CCT nd
A1 Stroma S45P TCT>CCT nd
A1 Muscle/fat S45P TCT>CCT nd
Initial right tumour
C2 Tumour pool ΔS45 ΔTCT nd
C2 Muscle I ΔS45 ΔTCT m/m
C2 Muscle II ΔS45 ΔTCT nd
C2 Normal kidney I wild type m/w
C2 Normal kidney II wild type nd
Recurrence left
3B Muscle I S45F TCT>TTT nd
3B Muscle II S45F TCT>TTT nd
Cell line S45F TCT>TTT m/m LOH 11p13 + p15 no LOH 11q11
Recurrence right
1E Blastema I S45C TCT>TGT nd LOH 11p13 no LOH 11q11
1E Blastema II S45C TCT>TGT nd
1E Muscle S45C TCT>TGT nd
1E Stroma S45C TCT>TGT nd
F1 Blastema I S45C TCT>TGT nd LOH 11p15
F1 Blastema II S45C TCT>TGT nd LOH 11p15
F1 Epithelia I wild type nd no LOH 11p15
F1 Epithelia II wild type nd no LOH 11p15
F1 Muscle S45C TCT>TGT nd LOH 11p15

Microdissected areas labelled in italics correspond to normal kidney cells by molecular analysis, one WT1 mutant allele as in all cells of the patient and no CTNNB1 mutation.

*WT1 mutation analysis was performed by sequencing, m/m indicates mutant/mutant allele, and m/w one mutant one wild type allele, nd: not done