ClinVar Miner

Submissions for variant NM_000540.3(RYR1):c.13153G>T (p.Asp4385Tyr)

dbSNP: rs1227202568
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001090644 SCV001246311 uncertain significance not provided 2020-01-01 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003987780 SCV004803733 uncertain significance not specified 2024-01-03 criteria provided, single submitter clinical testing Variant summary: RYR1 c.13153G>T (p.Asp4385Tyr) results in a non-conservative amino acid change in the encoded protein sequence. Five of five in-silico tools predict a damaging effect of the variant on protein function. The variant was absent in 103516 control chromosomes (gnomAD). The available data on variant occurrences in the general population are insufficient to allow any conclusion about variant significance. To our knowledge, no occurrence of c.13153G>T in individuals affected with RYR1-related disorders and no experimental evidence demonstrating its impact on protein function have been reported. One submitter has cited a clinical-significance assessment for this variant to ClinVar after 2014 and has classified the variant as uncertain significance. Based on the evidence outlined above, the variant was classified as uncertain significance.

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