ClinVar Miner

Submissions for variant NM_001377.3(DYNC2H1):c.10237C>G (p.Pro3413Ala)

dbSNP: rs786204223
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000168357 SCV000219046 uncertain significance Jeune thoracic dystrophy 2014-12-18 criteria provided, single submitter clinical testing In summary, this is a novel missense change with uncertain impact on protein function. It has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this sequence change is likely to be disruptive, but these predictions have not been confirmed by published functional studies. This sequence change has not been published in the literature and is not present in population databases. This sequence change replaces proline with alanine at codon 3420 of the DYNC2H1 protein (p.Pro3420Ala). The proline residue is highly conserved and there is a small physicochemical difference between proline and alanine.

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