ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.4024del (p.Trp1342fs)

dbSNP: rs1555093028
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000666761 SCV000791111 likely pathogenic Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 2017-04-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001389587 SCV001590982 pathogenic not provided 2022-09-27 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with MYO7A-related conditions. For these reasons, this variant has been classified as Pathogenic. ClinVar contains an entry for this variant (Variation ID: 551642). This variant is not present in population databases (gnomAD no frequency). This sequence change creates a premature translational stop signal (p.Trp1342Glyfs*57) in the MYO7A gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in MYO7A are known to be pathogenic (PMID: 8900236, 25404053).

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