ClinVar Miner

Submissions for variant NM_033380.3(COL4A5):c.936+1G>A

dbSNP: rs1569491107
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001379652 SCV001577490 likely pathogenic not provided 2022-05-14 criteria provided, single submitter clinical testing ClinVar contains an entry for this variant (Variation ID: 587199). 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. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. Disruption of this splice site has been observed in individual(s) with clinical features of Alport syndrome (PMID: 26809805). This variant is not present in population databases (gnomAD no frequency). This sequence change affects a donor splice site in intron 16 of the COL4A5 gene. It is expected to disrupt RNA splicing. Variants that disrupt the donor or acceptor splice site typically lead to a loss of protein function (PMID: 16199547), and loss-of-function variants in COL4A5 are known to be pathogenic (PMID: 9195222, 10752524, 14514738, 24854265, 26809805).

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