ClinVar Miner

Submissions for variant NM_017909.4(RMND1):c.703G>A (p.Val235Met)

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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 RCV003340962 SCV004047861 uncertain significance Combined oxidative phosphorylation defect type 11 criteria provided, single submitter clinical testing The missense variant in c.703G>A (p.Val235Met) in RMND1 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. The p.Val235Met 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.Val235Met in RMND1 is predicted as conserved by GERP++ and PhyloP across 100 vertebrates. The amino acid Val at position 235 is changed to a Met changing protein sequence and it might alter its composition and physico-chemical properties. For these reasons, this variant has been classified as Uncertain Significance (VUS).

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