List of variants in gene SIL1 reported as benign 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_022464.5(SIL1):c.153A>G (p.Thr51=)	rs3088052	0.50252
NM_022464.5(SIL1):c.-6C>G	rs11555154	0.06144
NM_022464.5(SIL1):c.1029+6T>C	rs57028146	0.02536
NM_022464.5(SIL1):c.394A>C (p.Lys132Gln)	rs61745568	0.02524
NM_022464.5(SIL1):c.239A>G (p.Gln80Arg)	rs35581768	0.00706
NM_022464.5(SIL1):c.454-6C>T	rs58624842	0.00601
NM_022464.5(SIL1):c.368C>T (p.Thr123Ile)	rs115800498	0.00470
NM_022464.5(SIL1):c.189T>G (p.Asp63Glu)	rs115591710	0.00413
NM_022464.5(SIL1):c.900C>T (p.Phe300=)	rs35080367	0.00410
NM_022464.5(SIL1):c.1030-14G>A	rs184154914	0.00148
NM_022464.5(SIL1):c.865-7C>T	rs141796576	0.00121
NM_022464.5(SIL1):c.573G>A (p.Lys191=)	rs148927511	0.00052
NM_022464.5(SIL1):c.1232G>A (p.Arg411His)	rs192255604	0.00020
NM_022464.5(SIL1):c.274C>T (p.Arg92Trp)	rs149242794	0.00009
NM_022464.5(SIL1):c.-11+21922C>T
NM_022464.5(SIL1):c.152_153inv (p.Thr51Met)
NM_022464.5(SIL1):c.353+19G>A
NM_022464.5(SIL1):c.615G>A (p.Ala205=)

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