ClinVar Miner

Submissions for variant NM_004415.4(DSP):c.6940G>T (p.Glu2314Ter) (rs1057518101)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000413488 SCV000491501 pathogenic not provided 2018-04-10 criteria provided, single submitter clinical testing The E2341X variant in the DSP gene has not been reported as a pathogenic variant or as a benign variant to our knowledge. The E2341X variant is predicted to cause loss of normal protein function by protein truncation as it results in a loss of the last 558 amino acids. Other nonsense variants in the DSP gene have been reported in HGMD in association with DSP-related disorders (Stenson et al., 2014). Furthermore, the E2341X pathogenic variant was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. In summary, E2341X in the DSP gene is expected to be pathogenic.

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