ClinVar Miner

Submissions for variant NM_006363.6(SEC23B):c.1142C>T (p.Thr381Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV004547257 SCV005042666 uncertain significance Congenital dyserythropoietic anemia, type II criteria provided, single submitter clinical testing The missense c.1142C>Tp.Thr381Ile variant in SEC23B gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Thr381Ile variant is novel not in any individuals in gnomAD Exomes and 1000 Genomes. This variant has not been reported to the ClinVar database. The amino acid change p.Thr381Ile in SEC23B is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Thr at position 381 is changed to a Ile changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as Variant of Uncertain Significance VUS.

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