ClinVar Miner

Submissions for variant NM_001384732.1(CPLANE1):c.1736C>T (p.Ala579Val)

gnomAD frequency: 0.00036  dbSNP: rs191239995
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252356 SCV000314174 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000646713 SCV000518589 benign not provided 2019-07-29 criteria provided, single submitter clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000625261 SCV000744332 benign Joubert syndrome 17 2017-10-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000646713 SCV000768492 benign not provided 2024-01-23 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000625261 SCV001315249 uncertain significance Joubert syndrome 17 2018-01-13 criteria provided, single submitter clinical testing This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.
Clinical Genetics, Academic Medical Center RCV000252356 SCV001918016 benign not specified no assertion criteria provided clinical testing

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