ClinVar Miner

Submissions for variant NM_018928.3(PCDHGC4):c.683_762del (p.Leu228fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology RCV002465045 SCV002759438 likely pathogenic Neurodevelopmental disorder with poor growth and skeletal anomalies 2022-08-23 criteria provided, single submitter clinical testing The c.683_762del variant is not present in publicly available population databases like 1000 Genomes, Exome Variant Server (EVS), Exome Aggregation Consortium (ExAC), Genome Aggregation Database (gnomAD) and Indian Exome Database. The variant is not present in our in-house exome database. This variant has not been published in literature or reported to clinical databases like ClinVar, Human Genome Mutation Database (HGMD) and OMIM, in any affected individuals. In-silico pathogenicity prediction programs like MutationTaster2, CADD, Varsome, Franklin etc. predicted this variant to be likely deleterious. The variant causes frameshift at the 228th amino acid position of the wild-type transcript which creates a translational premature stop signal at the 248th amino acid position of the altered transcript that either may causes nonsense mediated decay of the mRNA or results in translating a truncated protein.

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