ClinVar Miner

Submissions for variant NM_000528.4(MAN2B1):c.2431C>T (p.Leu811Phe)

gnomAD frequency: 0.00004  dbSNP: rs367852398
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001243581 SCV001416749 uncertain significance Deficiency of alpha-mannosidase 2023-12-02 criteria provided, single submitter clinical testing This sequence change replaces leucine, which is neutral and non-polar, with phenylalanine, which is neutral and non-polar, at codon 811 of the MAN2B1 protein (p.Leu811Phe). This variant is present in population databases (rs367852398, gnomAD 0.008%). This variant has not been reported in the literature in individuals affected with MAN2B1-related conditions. ClinVar contains an entry for this variant (Variation ID: 968446). 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 MAN2B1 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.
Natera, Inc. RCV001243581 SCV002086902 uncertain significance Deficiency of alpha-mannosidase 2020-06-06 no assertion criteria provided clinical testing

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