ClinVar Miner

Submissions for variant NM_014795.4(ZEB2):c.1601A>G (p.Asn534Ser)

dbSNP: rs767181131
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001221985 SCV001394063 uncertain significance Mowat-Wilson syndrome 2023-10-13 criteria provided, single submitter clinical testing This sequence change replaces asparagine, which is neutral and polar, with serine, which is neutral and polar, at codon 534 of the ZEB2 protein (p.Asn534Ser). This variant is present in population databases (rs767181131, gnomAD 0.006%). This variant has not been reported in the literature in individuals affected with ZEB2-related conditions. ClinVar contains an entry for this variant (Variation ID: 950301). Advanced modeling performed at Invitae incorporating data from internal and/or published experimental studies (Invitae) indicates that this missense variant is not expected to disrupt ZEB2 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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