ClinVar Miner

Submissions for variant NM_001379210.1(SLC25A26):c.596C>T (p.Pro199Leu)

dbSNP: rs869025315
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000207463 SCV000262736 pathogenic Combined oxidative phosphorylation deficiency 28 2016-02-11 no assertion criteria provided literature only

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