ClinVar Miner

Submissions for variant NM_153717.3(EVC):c.1068_1069del (p.Leu357fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV002309382 SCV002603193 likely pathogenic Ellis-van Creveld syndrome 2022-03-31 criteria provided, single submitter clinical testing NM_153717.2(EVC):c.1068_1069delAT(L357Vfs*26) is expected to be pathogenic in the context of EVC-related Ellis-van Creveld syndrome. This variant is predicted to lead to an abnormal or absent protein product due to the creation of a premature termination codon in EVC, a gene where loss-of-function variants are known to be pathogenic. Please note: this variant was assessed in the context of healthy population screening.

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