List of variants in gene combination NPHP3-ACAD11, UBA5 reported as likely pathogenic for cerebellar degeneration

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_024818.6(UBA5):c.542G>A (p.Cys181Tyr)
NM_024818.6(UBA5):c.562C>T (p.Arg188Ter)	rs374052333
NM_024818.6(UBA5):c.799C>T (p.Gln267Ter)	rs762779162

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