ClinVar Miner

Submissions for variant NM_001377.3(DYNC2H1):c.10157T>C (p.Ile3386Thr)

dbSNP: rs542490708
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000757202 SCV000885343 uncertain significance not provided 2018-04-20 criteria provided, single submitter clinical testing The DYNC2H1 c.10178T>C; p.Ile3393Thr variant (rs542490708), to our knowledge, is not reported in the medical literature, gene specific variation databases, nor has it been previously identified by our laboratory. This variant is listed in the genome Aggregation Database (gnomAD) with an overall population frequency of 0.0004 % (identified on 1 out of 245,870 chromosomes). The isoleucine at position 3393 is highly conserved, considering 28 species, and computational analyses of the effects of the p.Ile3393Thr variant on protein structure and function do not predict a deleterious effect (SIFT: benign, PolyPhen-2: tolerated). Based on the available information, the clinical significance of the p.Ile3393Thr variant cannot be determined with certainty.

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