ClinVar Miner

Submissions for variant NM_001081.3(CUBN):c.7400A>G (p.Asn2467Ser) (rs200197243)

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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 RCV000506010 SCV000603283 uncertain significance not provided 2017-05-25 criteria provided, single submitter clinical testing The p.Asn2467Ser variant (rs200197243) has not been reported in the medical literature, gene specific variation databases, nor has it been previously identified by our laboratory. This variant is listed in the NHLBI GO Exome Sequencing Project with an overall population frequency of 0.01 percent (identified on 1 out of 13006 chromosomes) and is listed in the Exome Aggregation Consortium Browser with an overall population frequency of 0.008 percent (identified on 10 out of 121050 chromosomes). The asparagine at position 2467 is highly conserved, up to Cow (considering 10 species) (Alamut v.2.9.0) and computational analyses of the effects of the p.Asn2467Ser variant on protein structure and function provide conflicting results (SIFT: tolerated, MutationTaster: disease causing, PolyPhen-2: benign). Altogether, there is not enough evidence to classify the p.Asn2467Ser variant with certainty.

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