ClinVar Miner

Submissions for variant NM_014402.5(UQCRQ):c.134C>T (p.Ser45Phe)

dbSNP: rs11544803
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000437264 SCV000517438 pathogenic not provided 2015-06-16 criteria provided, single submitter clinical testing The S45F variant in the UQCRQ gene has been reported previously in the homozygous state inassociation with mitochondrial complex III deficiency (Barel et al., 2008). The S45F substitution was notobserved at any significant frequency in approximately 6,500 individuals of European and AfricanAmerican ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variantin these populations. The S45F variant is a non-conservative amino acid substitution that is not conservedacross species. In silico analysis predicts this variant is probably damaging to the proteinstructure/function. We interpret S45F as a pathogenic variant.
OMIM RCV000000765 SCV000020915 pathogenic Mitochondrial complex III deficiency nuclear type 4 2008-05-01 no assertion criteria provided literature only

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