Submissions for variant NM_012330.4(KAT6B):c.5040C>G (p.Tyr1680Ter)

dbSNP: rs369027010

Total submissions: 1

Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego	RCV002246470	SCV001984830	pathogenic	Autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome; Brain small vessel disease 1 with or without ocular anomalies; Hemorrhage, intracerebral, susceptibility to; Retinal arterial tortuosity; Microangiopathy and leukoencephalopathy, pontine, autosomal dominant	2020-10-23	criteria provided, single submitter	clinical testing	This nonsense variant is found in the last exon of KAT6B-related disorders and it is therefore predicted to escape nonsense-mediated mRNA decay (NMD). This variant has not been previously reported or functionally characterized in the literature to our knowledge. However, nonsense variants located downstream of this variant have been reported as disease-causing variants in the Human Gene Mutation Database (PMID: 25424711, 22077973, 23436491, 28232779). It is absent from the gnomAD population database and thus is presumed to be rare. Analysis of the parental samples was negative for this variant, indicating this variant likely occurred as a de novo event. Based on the available evidence, the c.5040C>G (p.Tyr1680Ter) variant is classified as Pathogenic.