ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.1656del (p.Phe552fs)

dbSNP: rs1736795573
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001041854 SCV001205500 pathogenic Mitochondrial complex II deficiency, nuclear type 1; Paragangliomas 5 2019-12-11 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as Pathogenic. Loss-of-function variants in SDHA are known to be pathogenic (PMID: 22974104, 24781757). This variant has not been reported in the literature in individuals with SDHA-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change creates a premature translational stop signal (p.Phe552Leufs*20) in the SDHA gene. It is expected to result in an absent or disrupted protein product.

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