ClinVar Miner

Submissions for variant NM_004577.4(PSPH):c.301C>T (p.Arg101Ter)

dbSNP: rs1264747554
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
New York Genome Center RCV001256100 SCV001432887 likely pathogenic Seizure; Intellectual disability 2020-05-20 criteria provided, single submitter clinical testing The c.301C>T (p.Arg101Ter) variant identified in the PSPH gene leads to the premature termination of the protein at amino acid 101/226 (coding exon 6/8). This variant is absent from gnomAD suggesting it is not a common benign variant in the populations represented in this database. This variant is absent from ClinVar and to our current knowledge has not been reported in affected individuals in the literature. Whole genome sequencing did not identify a deep intronic or copy number variant in PSPH, although little is known regarding cisor transregulatory elements of this gene and very few patients have been reported to date. Given its deleterious nature and absence in population databases, the c.301C>T (p.Arg101Ter) variant identified in the PSPH gene is reported here as Likely Pathogenic.

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