ClinVar Miner

Submissions for variant NM_012470.4(TNPO3):c.2358G>A (p.Leu786=)

gnomAD frequency: 0.04242  dbSNP: rs11538884
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241741 SCV000311942 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV000241741 SCV000520475 benign not specified 2016-02-26 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Labcorp Genetics (formerly Invitae), Labcorp RCV001511363 SCV001718594 benign Autosomal dominant limb-girdle muscular dystrophy type 1F 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004712208 SCV005269443 benign not provided criteria provided, single submitter not provided

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