ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.861_862delinsCT (p.Gln287_Val288delinsHisLeu)

dbSNP: rs1555639508
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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 RCV000618138 SCV000738165 uncertain significance Cardiovascular phenotype 2017-09-18 criteria provided, single submitter clinical testing The c.861_862delGGinsCT variant (also known as p.Q287_V288delinsHL), located in coding exon 7 of the DSC2 gene, results from an in-frame deletion of GG and insertion of CT at nucleotide positions 861 to 862. This results in the substitution of glutamine and valine residues for a histidine and leucine residue at codon 287 and 288. These amino acid positions are not well conserved in available vertebrate species. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear.

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