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. 2020 Jul 28;10:12563. doi: 10.1038/s41598-020-69074-z

Table 2.

Germline pathogenic variants and somatic NF2 mutations and CNVs in the tumors.

Patient Sex Germline pathogenic variant Number of spinal meningiomas Number of cranial meningiomas Somatic mutation or CNV
P1 F Nonsense, exon11, c.1021C > T, p.R341X 4 5 Chr22 LOH in all tumors
P2 F Splice region, exon 2, c.241-9A > G 2 0 Chr22 LOH in both tumors
P3 F Nonsense, exon2, c.193C > T, p.Q65X 0 3 Chr22 LOH in all tumors
P4 F Nonsense, exon11, c.1030C > T, p.Q344X 3 0 Chr22 LOH in all tumors
P5 F Splice site, exon4, c.447+1G > T 1 0 Chr22 LOH
P6 M Nonsense, exon7, c.634C > T, p.Q212X 0 1 Chr22 LOH
P7 M Nonsense, exon8, c.784C > T, p.R262X 0 1 Frameshift, exon12, c.1234delC, p.Q412fs

LOH Loss of Heterozygosity.