ClinVar Miner

Submissions for variant NM_000186.4(CFH):c.3173_3182del (p.Ala1057_Tyr1058insTer)

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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 RCV003126313 SCV003802751 likely pathogenic Factor H deficiency; Hemolytic uremic syndrome, atypical, susceptibility to, 1 2023-01-20 criteria provided, single submitter clinical testing The c.3173_3182del variant is not present in publicly available population databases like 1000 Genomes, ExAC, EVS, gnomAD, Indian Exome Database and our in-house exome database. This variant has neither been published nor reported to clinical databases like ClinVar, Human Genome Mutation Database (HGMD) or OMIM, in any affected individuals. In silico pathogenicity prediction programs like MutationTaster2, CADD, Varsome, Franklin etc predicted this variant to be likely deleterious. This variant causes frameshift and creates a premature translational stop signal at the 1058th amino acid position of the wild-type transcript that may either result in translation of a truncated protein or cause nonsense-mediated decay of the mRNA.

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