ClinVar Miner

Submissions for variant NM_032237.5(POMK):c.407C>T (p.Thr136Met)

gnomAD frequency: 0.00006  dbSNP: rs138216719
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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 RCV000543765 SCV000654037 uncertain significance Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12; Limb-girdle muscular dystrophy due to POMK deficiency 2023-08-04 criteria provided, single submitter clinical testing 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 POMK 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. ClinVar contains an entry for this variant (Variation ID: 474191). This sequence change replaces threonine, which is neutral and polar, with methionine, which is neutral and non-polar, at codon 136 of the POMK protein (p.Thr136Met). This variant is present in population databases (rs138216719, gnomAD 0.04%). This variant has not been reported in the literature in individuals affected with POMK-related conditions.
Revvity Omics, Revvity RCV003133351 SCV003811798 uncertain significance not provided 2022-05-17 criteria provided, single submitter clinical testing

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