ClinVar Miner

Submissions for variant NM_007272.3(CTRC):c.667C>G (p.Gln223Glu)

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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 RCV002367001 SCV002661774 uncertain significance Hereditary pancreatitis 2022-04-20 criteria provided, single submitter clinical testing The p.Q223E variant (also known as c.667C>G), located in coding exon 7 of the CTRC gene, results from a C to G substitution at nucleotide position 667. The glutamine at codon 223 is replaced by glutamic acid, 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. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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