ClinVar Miner

Submissions for variant NM_000454.5(SOD1):c.239+6A>C

gnomAD frequency: 0.00022  dbSNP: rs374610141
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001289237 SCV001476920 benign not specified 2020-08-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002537988 SCV002983554 uncertain significance Amyotrophic lateral sclerosis type 1 2022-08-13 criteria provided, single submitter clinical testing This sequence change falls in intron 3 of the SOD1 gene. It does not directly change the encoded amino acid sequence of the SOD1 protein. It affects a nucleotide within the consensus splice site. This variant is present in population databases (rs374610141, gnomAD 0.06%). This variant has not been reported in the literature in individuals affected with SOD1-related conditions. ClinVar contains an entry for this variant (Variation ID: 995270). 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. 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.

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