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. Author manuscript; available in PMC: 2012 Nov 1.
Published in final edited form as: Mod Pathol. 2012 Feb 3;25(5):699–708. doi: 10.1038/modpathol.2011.208

Table 3.

Summary of PTEN exon sequence abnormalities (insertions, deletions, and point mutations) and endometrial carcinoma type.

ENDOMETRIOID NON-ENDOMETRIOID

All Sequence Abnormalities Detected n(%)1 Insertions and deletions Point Mutations All Sequence Abnormalities Detected n(%)1 Insertions and deletions Point Mutations
Exon 1 9 (12.9%) 5 4 5 (26.3%) 2 3
Exon 2 2 (2.9%) 0 2 0 (0%) 0 0
Exon 3 2 (2.9%) 0 2 0 (0%) 0 0
Exon 4 1 (1.4%) 0 1 1 (5.3%) 1 0
Exon 5 12 (17.1%) 4 8 4 (21.1%) 1 3
Exon 6 10 (14.3%) 5 5 0 (0%) 0 0
1 Exon 7 14 (20.0%) 10 4 1 (5.3%) 1 0
Exon 8 16 (22.9%) 7 9 5 (26.3%) 3 2
Exon 9 0 (0%) 0 0 1 (5.3%) 1 0
Exon 3 boundary 1 (1.4%) 1 0 0 (0%) 0 0
Exon 8 boundary 0 (0%) 0 0 1 (5.3%) 1 0
Splice region 6/7 2 (2.9%) 0 2 1 (5.3%) 0 1
Splice region 7/8 1 (1.4%) 0 1 0 (0%) 0 0

All 70 32 38 19 10 9
1

Exon 7 sequence abnormalities were significantly more common in endometrioid carcinomas compared to the non-endometrioid group (p=0.0199).