ClinVar Miner

Submissions for variant NM_018451.5(CENPJ):c.2872C>T (p.Arg958Ter) (rs749343808)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000497511 SCV000589826 likely pathogenic not provided 2016-04-20 criteria provided, single submitter clinical testing The R958X variant has not been published as a pathogenic variant, nor has it been reported as a benign variant to our knowledge. The R958X nonsense variant is predicted to cause loss of normal protein function either through protein truncation or nonsense-mediated mRNA decay. Furthermore, it was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. Although this variant has not been reported previously to our knowledge, another truncating variant downstream of this position has been reported in the Human Gene Mutation Database in association with a CENPJ-related disorder (Stenson et al., 2014). Therefore, this variant is likely pathogenic; however, the possibility that it is benign cannot be excluded. GeneDx interprets R958X as a likely pathogenic variant.
Fulgent Genetics,Fulgent Genetics RCV000762911 SCV000893323 pathogenic Primary autosomal recessive microcephaly 6; Seckel syndrome 4 2018-10-31 criteria provided, single submitter clinical testing

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