ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.9287-27_9287-2del

dbSNP: rs1064792968
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000462643 SCV000550324 likely pathogenic Duchenne muscular dystrophy 2020-01-07 criteria provided, single submitter clinical testing In summary, the currently available evidence indicates that the variant is pathogenic, but additional data are needed to prove that conclusively. Therefore, this variant has been classified as Likely Pathogenic. Nucleotide substitutions within the consensus splice site are a relatively common cause of aberrant splicing (PMID: 17576681, 9536098). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site, but this prediction has not been confirmed by published transcriptional studies. This variant has been observed in individual(s) with clinical features of Duchenne muscular dystrophy (Invitae). ClinVar contains an entry for this variant (Variation ID: 409934). This variant is not present in population databases (ExAC no frequency). This sequence change falls in intron 63 of the DMD gene. It does not directly change the encoded amino acid sequence of the DMD protein, but it affects a nucleotide within the consensus splice site of the intron.

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