ClinVar Miner

Submissions for variant NM_000153.4(GALC):c.287A>G (p.His96Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV001357746 SCV001553307 uncertain significance not provided no assertion criteria provided clinical testing The GALC p.H96R variant was not identified in the literature nor was it identified in ClinVar. The variant was identified in dbSNP (ID: rs748593957) and in control databases in 3 of 249404 chromosomes at a frequency of 0.00001203 (Genome Aggregation Database March 6, 2019, v2.1.1). The p.H96 residue is conserved in mammals and computational analyses (MUT Assesor, PolyPhen-2, SIFT, MutationTaster, Revel, FATHMM, MetaLR, DANN) suggest that the variant may impact the protein; however, this information is not predictive enough to assume pathogenicity. The variant occurs outside of the splicing consensus sequence and in silico or computational prediction software programs (Splice AI exome and Splice AI genome) do not predict a deleterious effect on splicing. In summary, based on the above information the clinical significance of this variant cannot be determined with certainty at this time. This variant is classified as a variant of uncertain significance.

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