ClinVar Miner

Submissions for variant NM_005006.7(NDUFS1):c.1651G>T (p.Asp551Tyr)

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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 RCV003448749 SCV004176430 uncertain significance Mitochondrial complex 1 deficiency, nuclear type 5 2023-03-01 criteria provided, single submitter clinical testing The missense c.1651G>T(p.Asp551Tyr) variant in NDUFS1 gene has not been reported previously as a pathogenic variant nor a benign variant, to our knowledge. The p.Asp551Tyr 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.Asp551Tyr in NDUFS1 is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Asp at position 551 is changed to a Tyr 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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