ClinVar Miner

Submissions for variant NM_000375.3(UROS):c.56A>G (p.Tyr19Cys)

dbSNP: rs1590007244
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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 RCV000856826 SCV000999248 pathogenic Cutaneous porphyria 2019-09-19 criteria provided, single submitter clinical testing The Tyr19Cys variant is not present in any publicly available databases like 1000 Genomes, Exome Variant Server (EVS), Exome Aggregation Consortium (ExAC), Genome Aggregation Database (gnomAD) and dbSNP. The variant is also not present in our in-house exome database. This variant was reported earlier in affected individuals with similar phenotype in Human Genome Mutation Database (CM951262) [Xu et al., J Clin Invest 1995]. In-silico pathogenicity prediction programs like SIFT, Polyphen2, Mutation Taster2, CADD etc. predicted this variant as likely disease causing. As per the ACMG guidelines the variant has been classified as pathogenic.

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