ClinVar Miner

Submissions for variant NM_005654.6(NR2F1):c.32C>T (p.Pro11Leu)

dbSNP: rs1276892077
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001917336 SCV002149982 uncertain significance not provided 2022-10-04 criteria provided, single submitter clinical testing This variant is not present in population databases (gnomAD no frequency). 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) performed at Invitae indicates that this missense variant is not expected to disrupt NR2F1 protein function. ClinVar contains an entry for this variant (Variation ID: 1380872). This variant has not been reported in the literature in individuals affected with NR2F1-related conditions. This sequence change replaces proline, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 11 of the NR2F1 protein (p.Pro11Leu).

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