ClinVar Miner

Submissions for variant NM_014797.3(ZBTB24):c.620T>C (p.Leu207Pro)

gnomAD frequency: 0.00001  dbSNP: rs762302021
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001210806 SCV001382314 uncertain significance Immunodeficiency-centromeric instability-facial anomalies syndrome 2 2022-05-29 criteria provided, single submitter clinical testing This sequence change replaces leucine, which is neutral and non-polar, with proline, which is neutral and non-polar, at codon 207 of the ZBTB24 protein (p.Leu207Pro). This variant is present in population databases (rs762302021, gnomAD 0.004%). This variant has not been reported in the literature in individuals affected with ZBTB24-related conditions. ClinVar contains an entry for this variant (Variation ID: 941092). 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 proline 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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