ClinVar Miner

Submissions for variant NM_000021.4(PSEN1):c.514_516TTG[1] (p.Leu174del)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics RCV000850226 SCV000965587 uncertain significance Alzheimer disease, type 3; Frontotemporal dementia 2019-06-27 criteria provided, single submitter clinical testing A heterozygous variant c.517_519delTTG (p.Leu174del) in Exon-6 has been observed in the PSEN1 gene. The proband, born of a non-consanguineous marriage, presented with clinical indication of progressive memory loss and behavioral changes. Her MRI of brain showed diffuse cerebral and cerebellar atrophy, frontal and temporal lobe atrophy. Her multiple family members have similar symptoms. The patient in our clinical analysis was observed with the said variant in an autosomal dominant mode of inheritance. The variant has not been reported in the 1000 genomes and ExAC databases. The in-silico predictions of the variant are probably damaging by MutationTaster2. In summary, the said variant meets our criteria to be classified as uncertain significance based on the mode of inheritance, in silico prediction, allele frequency in population databases and lack of segregation study.

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