ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.162G>A (p.Gln54=)

gnomAD frequency: 0.00001  dbSNP: rs1468436658
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000649463 SCV000771291 likely benign Mitochondrial complex II deficiency, nuclear type 1; Paragangliomas 5 2023-09-19 criteria provided, single submitter clinical testing
Ambry Genetics RCV002397292 SCV002708121 likely benign Hereditary cancer-predisposing syndrome 2022-05-21 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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