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Fig. 5 | Human Genomics

Fig. 5

From: Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach

Fig. 5

Variants identified per family in all 11 genomes from the two families under study. The DM (disease-causing mutations) and DM? (putative disease-causing mutations but where there is some residual doubt as to pathological significance) mutations identified as well as our two variants of prime interest, MSH2 c.2732T>A and BRCA1 c.2955delC, are shown

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Human Genomics

ISSN: 1479-7364