ClinVar Miner

Submissions for variant NM_001044385.3(TMEM237):c.137-3T>C

gnomAD frequency: 0.00002  dbSNP: rs540193518
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001059254 SCV001223874 uncertain significance Joubert syndrome 14 2023-08-28 criteria provided, single submitter clinical testing This variant has not been reported in the literature in individuals affected with TMEM237-related conditions. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Variants that disrupt 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 is not likely to affect RNA splicing. ClinVar contains an entry for this variant (Variation ID: 854245). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This sequence change falls in intron 4 of the TMEM237 gene. It does not directly change the encoded amino acid sequence of the TMEM237 protein. It affects a nucleotide within the consensus splice site.

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