“…The obvious predominance of missense over non-missense mutations is, however, only seen between codons 130 and 286 (Greenblatt et al, 1994). In an earlier study of p53 mutations in SCCHN we found a deletion of 14 bp in exon 8 in one tumour (Nylander et al, 1995). Big deletions have been reported in other studies of SCCHN (Ahomadegbe et al, 1995;Magnusson et al, 1995;Zariwala et al, 1994) as well as in other tumours, such as colon cancer, breast cancer, leukaemia and oesophageal carcinoma (Jego et al, 1993;Huang et al, 1994).…”