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J Med Genet 39:315-322 doi:10.1136/jmg.39.5.315
  • Original article

Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas

Table 4

SSCP/HA analysis and LOH studies on lymphocyte and tumour samples from 30 young patients with a unilateral vestibular schwannoma

SSCP/HA LOH analysis
Case Tissue Mutation Class D22S275 NF2CA3 D22S268 D22S280
Tissue: L = lymphocyte DNA, T = tumour DNA.
SSCP/HA: F = frameshift, SP = splice site, N = nonsense, M = missense, IF = in frame deletion, SY = synonymous codon substitution, – = no mutation, * = insufficient material for complete analysis.
LOH analysis: LOH = loss of heterozygosity, U = uninformative, N = no loss of heterozygosity, NR = no result, – = not tested.
1 L -ve
T 1080ΔG F LOH LOH LOH
2 L 465C>T SY
T Δ757-795 (ΔLys253>Ser265) IF LOH LOH
3 L -ve
T 1443C>G (Tyr481>Stop) N LOH U LOH
4 L -ve
T 459C>A (Tyr153>Stop) N LOH N
5 L -ve
T 448-1g>t SP LOH
6 L -ve
T 1228C>T (Gln433>Stop) N U U N
7 L -ve
T 970C>T (Gln324>Stop) N LOH U LOH
8 L -ve
T -ve LOH U LOH
9 L Δ332-334 (ΔGlu112) IF
T 459C>G (Tyr153>Stop) N LOH U LOH
10 L -ve
T1 169C>T (Arg57>Stop) N LOH U U
655G>A (Val219>Met) M
1600ΔC F
T2 655G>A (Val219>Met) M N U U
11 L -ve
T 1514ΔTG F LOH
12 L -ve
T 479ΔG F LOH U LOH
13 L -ve
T Δ171-216 F NR N N
14 L -ve
T -ve for 16/17 exons* LOH
15 L -ve
T 1513ΔCTGT F LOH U U
16 L -ve
T 169C>T (Arg57>Stop) N LOH
17 L -ve
T -ve LOH
18 L -ve
T -ve for 5/17 exons*
19 L -ve
T insufficient material
20 L -ve
T 1621ΔG F LOH
21 L -ve
T nt 1366 C>T (Glyn 456>stop) LOH
22 L -ve
T 447+2t>c SP N U U
23 L -ve
T 653ΔG F LOH
24 L -ve
T 54insA F LOH
25 L -ve
T -ve LOH
26 L -ve
T 737ΔC F N
nt 810 g>a SP
27 L -ve
T -ve N
28 L -ve
T -ve N
29 L -ve
T 265insG F LOH
30 L -ve
T -ve U U U

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