ClinVar Miner

Submissions for variant NM_001754.5(RUNX1):c.349A>G (p.Lys117Glu)

dbSNP: rs2146407735
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinGen Myeloid Malignancy Variant Curation Expert Panel RCV004719206 SCV005326430 uncertain significance Hereditary thrombocytopenia and hematologic cancer predisposition syndrome 2024-09-16 reviewed by expert panel curation NM_001754.5(RUNX1):c.349A>G (p.Lys117Glu) is a missense variant which has a REVEL score ≥ 0.88 (0.95) (PP3). This missense variant is located within the Runt Homology Domain (AA 89-204), but does not occur in an established hotspot residue (PM1_supporting). This variant is completely absent from all population databases with at least 20x coverage for RUNX1 (PM2_supporting). In summary, the clinical significance of this variant is uncertain. ACMG/AMP criteria applied, as specified by the Myeloid Malignancy Variant Curation Expert Panel for RUNX1: PP3, PM1_supporting, PM2_supporting.
Labcorp Genetics (formerly Invitae), Labcorp RCV001965248 SCV002211639 uncertain significance Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1 2021-07-09 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. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Tolerated"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Class C0"). This variant has not been reported in the literature in individuals affected with RUNX1-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change replaces lysine with glutamic acid at codon 117 of the RUNX1 protein (p.Lys117Glu). The lysine residue is moderately conserved and there is a small physicochemical difference between lysine and glutamic acid.

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