Skip to main content
Figure 3 | Orphanet Journal of Rare Diseases

Figure 3

From: Germline SMARCA4 mutations in patients with ovarian small cell carcinoma of hypercalcemic type

Figure 3

A pedigree of the proband’s 1 family. The proband (P, II:1) with SCCHT had a germline mutation in SMARCA4 exon 26 (c.3760G > T) inherited from her father (I:1). This mutation was also identified in the proband’s two sons (III:1, III:2), sister (II:3) and in the sister’s two children (III:3, III:4). (+/−) heterozygous mutation carrier in the germline; (+/+) wild-type in the germline. A diagonal line through a symbol indicates that the person is deceased.

Back to article page