ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.3233C>T (p.Thr1078Ile)

dbSNP: rs2056875659
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001968215 SCV002237527 uncertain significance Achondrogenesis, type IA 2022-09-07 criteria provided, single submitter clinical testing This sequence change replaces threonine with isoleucine at codon 1078 of the TRIP11 protein (p.Thr1078Ile). The threonine residue is weakly conserved and there is a moderate physicochemical difference between threonine and isoleucine. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Not Available"; PolyPhen-2: "Benign"; Align-GVGD: "Not Available"). ClinVar contains an entry for this variant (Variation ID: 1461956). This variant has not been reported in the literature in individuals affected with TRIP11-related conditions. This variant is not present in population databases (gnomAD no frequency).

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