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. 2012 Jan 25;7(1):e30418. doi: 10.1371/journal.pone.0030418

Table 1. Loss of heterozygosity (LOH) and mutation in sporadic vestibular schwannomas.

No Exon DNA sequence alteration Codon change Consequence LOH
D22S268 D22S275 D22S929
1 2 c.136T>G (p.L46R) 46 Missense + + +
2 3 c.363+1G>A - Splicing donor site + + +
3 - - - - + + +
4 2, 3 c.232_233 ins G c.303T>A (p.Y101X) 78 101 Frameshift, Nonsense
6 3 c.280 del T 94 Frameshift + + +
8 2 c.122G>A (p.W41X) 41 Nonsense
10 13 c.1379 del T 460 Frameshift
12 2 c.169C>T (p.R57X) 57 Nonsense + + +
13 12 c.133 C>G (p.S444X) 444 Nonsense + + +
14 - - - - + + +
15 2 c.154_175del22 51–59 Frameshift
17 10 c.955C>T (p.Q319X) 319 Nonsense
21 10 c.963_964 ins A 322 Frameshift +
22 14 c.1568_1574+7del14 523–525+intron7bp Frameshift
24 7, 8 c.616G>T (p.E206X) c.694_771del78 206 232–257 Nonsense In-frame deletion
27 4 c.364-8_408del53 Intron8bp+122–136 Frameshift
29 2 c.169C>T (p.R57X) 57 Nonsense
30 4 c.394 delT 132 Frameshift + + +