ClinVar Miner

Submissions for variant NM_024642.5(GALNT12):c.1451A>G (p.Gln484Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV004623711 SCV005119869 uncertain significance not specified 2024-03-17 criteria provided, single submitter clinical testing The p.Q484R variant (also known as c.1451A>G), located in coding exon 8 of the GALNT12 gene, results from an A to G substitution at nucleotide position 1451. The glutamine at codon 484 is replaced by arginine, an amino acid with highly similar properties. This amino acid position is conserved. In addition, this alteration is predicted to be tolerated by in silico analysis. Based on the available evidence, the clinical significance of this alteration remains unclear.

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