ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.586C>T (p.Gln196Ter) (rs149079426)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000778421 SCV000914659 uncertain significance Achondrogenesis, type IA 2017-04-28 criteria provided, single submitter clinical testing The TRIP11 c.586C>T (p.Gln196Ter) variant is a stop-gained variant predicted to result in premature termination of the protein. The variant was observed by ICSL 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 for this variant, it 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. No publications were found based on this search. Due to the potential impact of stop-gained variants and the lack of clarifying evidence, this variant is classified as a variant of unknown significance but suspicious for pathogenicity for achondrogenesis.
SIB Swiss Institute of Bioinformatics RCV000853509 SCV000996457 pathogenic Goldblatt hypertension 2019-06-27 criteria provided, single submitter curation This variant is interpreted as a Pathogenic for Odontochondrodysplasia, autosomal recessive. The following ACMG Tag(s) were applied: PM2, PVS1, PM3-Strong.
OMIM RCV000757982 SCV000886531 pathogenic Osteochondrodysplasia 2019-02-26 no assertion criteria provided literature only

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