ClinVar Miner

Submissions for variant NM_024642.5(GALNT12):c.1156G>A (p.Val386Ile)

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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 RCV004924208 SCV005593884 uncertain significance not specified 2024-09-30 criteria provided, single submitter clinical testing The p.V386I variant (also known as c.1156G>A), located in coding exon 6 of the GALNT12 gene, results from a G to A substitution at nucleotide position 1156. The valine at codon 386 is replaced by isoleucine, an amino acid with highly similar properties. This amino acid position is conserved. In addition, the in silico prediction for this alteration is inconclusive. Based on the available evidence, the clinical significance of this variant remains unclear.

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