ClinVar Miner

Submissions for variant NM_003011.4(SET):c.663+5G>C

dbSNP: rs1861628072
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001067044 SCV001232074 pathogenic not provided 2021-02-24 criteria provided, single submitter clinical testing For these reasons, this variant has been classified as 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 SET-related intellectual disability (Invitae). In at least one individual the variant was observed to be de novo. This variant is not present in population databases (ExAC no frequency). This sequence change falls in intron 6 of the SET gene. It does not directly change the encoded amino acid sequence of the SET protein. It affects a nucleotide within the consensus splice site of the intron.
Undiagnosed Diseases Network, NIH RCV002252311 SCV002523177 pathogenic Intellectual disability, autosomal dominant 58 2021-02-25 criteria provided, single submitter clinical testing

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