ClinVar Miner

Submissions for variant NM_006397.3(RNASEH2A):c.866del (p.Leu289fs)

dbSNP: rs1969104623
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001227635 SCV001400001 uncertain significance Aicardi-Goutieres syndrome 4 2019-10-15 criteria provided, single submitter clinical testing This sequence change results in a frameshift in the RNASEH2A gene (p.Leu289Argfs*27). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 11 amino acids of the RNASEH2A protein and extend the protein by an additional 16 amino acids. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with RNASEH2A-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. 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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