rs779293116

Description

This sequence change falls in intron 2 of the RNASEH2C gene. It does not directly change the encoded amino acid sequence of the RNASEH2C protein. It affects a nucleotide within the consensus splice site of the intron. This variant is present in population databases (rs779293116, ExAC 0.03%). This variant has not been reported in the literature in individuals affected with RNASEH2C-related conditions. ClinVar contains an entry for this variant (Variation ID: 305362). 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.