ClinVar Miner

Submissions for variant NM_003482.4(KMT2D):c.16391_16392insAG (p.Leu5465fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV002505982 SCV002817307 pathogenic not provided 2020-10-16 criteria provided, single submitter clinical testing KMT2D frameshift variants are known to be pathogenic and multiple frameshift variants in this region have been reported in Kabuki syndrome 1 patients (PMID: 21671394). This variant occurred de novo in an individual tested at Athena Diagnostics, who had clinical features consistent with this gene. This variant has not been reported in large, multi-ethnic general populations (http://gnomad.broadinstitute.org).This observation is not an independent occurrence and has been identified in the same individual by RCIGM, the other laboratory participating in the GEMINI study.

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