ClinVar Miner

Submissions for variant NM_004369.4(COL6A3):c.8467=

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000598576 SCV000710691 likely pathogenic not provided 2018-02-15 criteria provided, single submitter clinical testing The c.8465-13_8467del16ins16 variant in the COL6A3 gene has not been reported previously as a pathogenic variant nor as a benign variant, to our knowledge. This variant results in the deletion of 16 nucleotides and the insertion of 16 nucleotides at the exon 13/intron 13 boundary, which destroys the canonical splice acceptor site in intron 13. This splice site variant is predicted to cause abnormal gene splicing resulting in an in-frame protein product with an abnormal message. However, in the absence of RNA/functional studies, the actual effect of c.8465-13_8467del16ins16 in this individual is unknown. The c.8465-13_8467del16ins16 variant is not observed in large population cohorts (Lek et al., 2016). We interpret c.8465-13_8467del16ins16 as a likely pathogenic variant.

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