ClinVar Miner

Submissions for variant NM_012330.4(KAT6B):c.2666C>A (p.Ser889Tyr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV004738988 SCV005341754 uncertain significance KAT6B-related disorder 2024-04-17 no assertion criteria provided clinical testing The KAT6B c.2666C>A variant is predicted to result in the amino acid substitution p.Ser889Tyr. To our knowledge, this variant has not been reported in the literature or in a large population database, indicating this variant is rare. At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence.

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