ClinVar Miner

Submissions for variant NM_005691.3(ABCC9):c.2848A>T (p.Met950Leu) (rs1448325219)

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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 RCV000756945 SCV000884938 uncertain significance not provided 2018-03-25 criteria provided, single submitter clinical testing The ABCC9 c.2848A>T; p.Met950Leu variant, 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 absent from the general population databases (1000 Genomes Project, Exome Variant Server, Genome Aggregation Database), indicating it is not a common polymorphism. The methionine at position 950 is weakly conserved, considering 12 species, and computational analyses of the effects of the p.Met950Leu variant on protein structure and function do not predict a deleterious effect (SIFT: tolerated , PolyPhen-2: benign). Based on the available information, the clinical significance of the p.Met950Leu variant cannot be determined with certainty.

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