ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.4754G>A (p.Arg1585His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003070446 SCV003476680 uncertain significance Achondrogenesis, type IA 2023-07-07 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with TRIP11-related conditions. 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. Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) has been performed at Invitae for this missense variant, however the output from this modeling did not meet the statistical confidence thresholds required to predict the impact of this variant on TRIP11 protein function. ClinVar contains an entry for this variant (Variation ID: 2162835). This variant is present in population databases (rs771459106, gnomAD 0.1%). This sequence change replaces arginine, which is basic and polar, with histidine, which is basic and polar, at codon 1585 of the TRIP11 protein (p.Arg1585His).

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