ClinVar Miner

Submissions for variant NM_022455.5(NSD1):c.3178C>G (p.Pro1060Ala)

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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 RCV004547226 SCV005042608 uncertain significance Sotos syndrome criteria provided, single submitter clinical testing The missense c.3178C>G p.Pro1060Ala variant in NSD1 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Pro1060Ala 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.Pro1060Ala in NSD1 is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Pro at position 1060 is changed to a Ala changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as a Variant of Uncertain Significance VUS.

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