List of variants in gene STUB1 reported as uncertain significance for cerebellar disorder

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_005861.4(STUB1):c.433A>C (p.Lys145Gln)	rs146251364	0.00063
NM_005861.4(STUB1):c.518G>T (p.Arg173Leu)	rs755346712	0.00001
NM_005861.4(STUB1):c.134C>A (p.Ala45Glu)	rs2151503733
NM_005861.4(STUB1):c.154G>A (p.Ala52Thr)	rs2151503748
NM_005861.4(STUB1):c.391T>C (p.Phe131Leu)	rs2151504534
NM_005861.4(STUB1):c.427AAG[2] (p.Lys145del)	rs779647632
NM_005861.4(STUB1):c.460C>T (p.Arg154Cys)

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