Description
Published functional studies demonstrate a damaging effect: loss of growth suppression and transcriptional activation activities, with a dominant-negative effect observed (Flaman et al., 1998; Ashur-Fabian et al., 2007; Dearth et al., 2007; Kotler et al., 2018; Giacomelli et al., 2018); In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Not observed at significant frequency in large population cohorts (gnomAD); This variant is associated with the following publications: (PMID: 26585234, 10753186, 22427690, 15161705, 28315634, 12726864, 2113594, 21190917, 20966976, 9400993, 18689542, 24446311, 25431194, 26230955, 25287991, 21483000, 21113594, 18555592, 11051241, 10519380, 17646286, 17875924, 10567903, 12792784, 14559903, 9546439, 16861262, 26552420, 20182602, 20407015, 11297255, 25148739, 17361096, 26619011, 16778209, 17311302, 22089350, 31050713, 30840781, 15302922, 29979965, 15510160, 32817165, 30224644, 33138793)
# | Sample | Method | Observation |
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Origin | Affected | Number tested | Tissue | Purpose | Method | Individuals | Allele frequency | Families | Co-occurrences |
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1 | germline | yes | not provided | not provided | not provided | | not provided | not provided | not provided | not provided |