ClinVar Miner

Submissions for variant NM_032638.5(GATA2):c.466G>C (p.Val156Leu)

dbSNP: rs2068695139
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001957026 SCV002251404 uncertain significance Deafness-lymphedema-leukemia syndrome; Monocytopenia with susceptibility to infections 2021-04-11 criteria provided, single submitter clinical testing 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 GATA2 protein function. This variant has not been reported in the literature in individuals with GATA2-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces valine with leucine at codon 156 of the GATA2 protein (p.Val156Leu). The valine residue is weakly conserved and there is a small physicochemical difference between valine and leucine.
Baylor Genetics RCV004571769 SCV005058900 uncertain significance Acute myeloid leukemia 2024-01-26 criteria provided, single submitter clinical testing

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