ClinVar Miner

Submissions for variant NM_001368809.2(AMPD2):c.1863-7C>G

dbSNP: rs563578390
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001969759 SCV002224893 uncertain significance Hereditary spastic paraplegia 63; Pontocerebellar hypoplasia type 9 2021-08-31 criteria provided, single submitter clinical testing 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. Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. This variant has not been reported in the literature in individuals affected with AMPD2-related conditions. This variant is not present in population databases (ExAC no frequency). This sequence change falls in intron 15 of the AMPD2 gene. It does not directly change the encoded amino acid sequence of the AMPD2 protein.

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