ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.1084G>T (p.Asp362Tyr)

dbSNP: rs2126584224
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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 RCV001360847 SCV001556794 uncertain significance Mitochondrial complex II deficiency, nuclear type 1; Paragangliomas 5 2020-06-15 criteria provided, single submitter clinical testing This sequence change replaces aspartic acid with tyrosine at codon 362 of the SDHA protein (p.Asp362Tyr). The aspartic acid residue is highly conserved and there is a large physicochemical difference between aspartic acid and tyrosine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with SDHA-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be disruptive, but these predictions have not been confirmed by published functional studies and their clinical significance is uncertain. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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