ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.5143GAG[1] (p.Glu1716del)

dbSNP: rs1555102843
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003230352 SCV003928884 pathogenic Usher syndrome 2023-04-27 criteria provided, single submitter clinical testing Variant summary: MYO7A c.5146_5148delGAG (p.Glu1716del) results in an in-frame deletion that is predicted to remove 1 amino acid from the encoded protein. The variant was absent in 159352 control chromosomes. c.5146_5148delGAG has been reported in the literature in multiple individuals affected with autosomal recessive non-syndromic congenital deafness with evidence of segregation (example: Riazuddin_2008). These data indicate that the variant is very likely to be associated with disease. GFP-myosin VIIa protein engineered to have an equivalent DFNB2 mutation to p.E1716del localizes correctly in transfected mouse hair cells, suggesting potentially less severe phenotype (Riazuddin_2008). The following publication has been ascertained in the context of this evaluation (PMID: 18181211). One clinical diagnostic laboratory has submitted clinical-significance assessments for this variant to ClinVar after 2014 without evidence for independent evaluation. One laboratory classified the variant as pathogenic. Based on the evidence outlined above, the variant was classified as pathogenic.
OMIM RCV000012639 SCV000032874 pathogenic Autosomal recessive nonsyndromic hearing loss 2 2008-04-01 no assertion criteria provided literature only

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