ClinVar Miner

Submissions for variant NM_001384732.1(CPLANE1):c.1828C>T (p.Gln610Ter)

gnomAD frequency: 0.00001  dbSNP: rs1200574734
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
3billion RCV001808116 SCV002058598 likely pathogenic Orofaciodigital syndrome type 6 2022-01-03 criteria provided, single submitter clinical testing Stop-gained (nonsense): predicted to result in a loss or disruption of normal protein function through nonsense-mediated decay (NMD) or protein truncation. Multiple pathogenic variants are reported downstream of the variant (PVS1_VS). It is not observed in the gnomAD v2.1.1 dataset (PM2_M). Therefore, this variant is classified as likely pathogenic according to the recommendation of ACMG/AMP guideline.

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