ClinVar Miner

Submissions for variant NM_053025.4(MYLK):c.5392G>A (p.Glu1798Lys)

dbSNP: rs777616795
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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 RCV000756400 SCV000884200 uncertain significance not provided 2018-01-28 criteria provided, single submitter clinical testing The MYLK c.5392G>A; p.Glu1798Lys variant (rs777616795), 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 245,864 chromosomes). The glutamic acid at position 1798 is moderately conserved, considering 12 species, and computational analyses of the effects of the p.Glu1798Lys variant on protein structure and function make conflicting predictions (SIFT: tolerated, MutationTaster: disease causing, PolyPhen-2: probably damaging). Based on the available information, the clinical significance of the p.Glu1798Lys variant cannot be determined with certainty.

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