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Fig. 2 | Hereditary Cancer in Clinical Practice

Fig. 2

From: Two novel sequence variants in MSH2 gene in a patient who underwent cancer genetic counseling for a very early-onset epithelial ovarian cancer

Fig. 2

The heterozygous state for the mutations (c.1706A > T) and (c.1711G > T) at exon 11 of MSH2 gene. a MSH2 genomic sequence analysis (fragment including exon 11) showing the two mutations identified in our index case. The arrow indicates the position of two mutations. b MSH2 cDNA sequence analysis (fragment including exons 9–15) showing the two mutations at mRNA level. The arrow indicates the lowering peak of mutant allele

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Hereditary Cancer in Clinical Practice

ISSN: 1897-4287