ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.5971_5973del (p.Asp1991del)

dbSNP: rs1278877639
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001066166 SCV001231167 uncertain significance Charcot-Marie-Tooth disease axonal type 2O 2022-05-25 criteria provided, single submitter clinical testing In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. ClinVar contains an entry for this variant (Variation ID: 859945). This variant has not been reported in the literature in individuals affected with DYNC1H1-related conditions. This variant is present in population databases (no rsID available, gnomAD 0.0009%). This variant, c.5971_5973del, results in the deletion of 1 amino acid(s) of the DYNC1H1 protein (p.Asp1991del), but otherwise preserves the integrity of the reading frame.

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