ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.157C>A (p.Pro53Thr)

dbSNP: rs782656592
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000480059 SCV000573207 uncertain significance not provided 2018-11-27 criteria provided, single submitter clinical testing A variant of uncertain significance has been identified in the LAMA4 gene. The P53T variant has not been published as pathogenic or been reported as benign to our knowledge. This variant is not observed in large population cohorts (Lek et al., 2016; 1000 Genomes Consortium et al., 2015; Exome Variant Server). The P53T variant is a non-conservative amino acid substitution, which is likely to impact secondary protein structure as these residues differ in polarity, charge, size and/or other properties. However, this substitution occurs at a position that is not conserved across species and in silico analysis suggests that this variant likely does not alter the protein structure/function.

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