ClinVar Miner

Submissions for variant NM_001080517.3(SETD5):c.1441-1G>A

dbSNP: rs2041850171
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV001174534 SCV001250896 pathogenic Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency 2020-05-18 criteria provided, single submitter clinical testing The variant c.1441-1G>A in SETD5 leads to the alteration of the canonical WT acceptor site, most probably affecting splicing. To our knowledge, the variant is not found in databases (gnomAD / ExAC). The phenotype described in OMIM and present literature matched the phenotype of our affected patient very well. The variant was inherited by our patient from the mother, who was clinically not assessed (asymptomatic carrier mothers of pathogenic SETD5 variants have already been described, as in Powis et al. (2018), PMID: 28881385). ACMG criteria used for classification: PVS1, PM2.

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