ClinVar Miner

Submissions for variant NM_004239.4(TRIP11):c.4712G>A (p.Arg1571His)

gnomAD frequency: 0.00001  dbSNP: rs534500568
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000593250 SCV000705619 uncertain significance not provided 2017-02-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002483613 SCV002782835 uncertain significance Achondrogenesis, type IA; Odontochondrodysplasia 1 2021-10-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002532488 SCV003448527 uncertain significance Achondrogenesis, type IA 2022-05-19 criteria provided, single submitter clinical testing This sequence change replaces arginine, which is basic and polar, with histidine, which is basic and polar, at codon 1571 of the TRIP11 protein (p.Arg1571His). This variant is present in population databases (rs534500568, gnomAD 0.0009%). This variant has not been reported in the literature in individuals affected with TRIP11-related conditions. ClinVar contains an entry for this variant (Variation ID: 499894). Algorithms developed to predict the effect of missense changes on protein structure and function output the following: SIFT: "Not Available"; PolyPhen-2: "Benign"; Align-GVGD: "Not Available". The histidine amino acid residue is found in multiple mammalian species, which suggests that this missense change does not adversely affect protein function. 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.

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