List of variants in gene PRKCG reported as likely benign 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_002739.5(PRKCG):c.285C>T (p.Asp95=)	rs17854523	0.03329
NM_002739.5(PRKCG):c.1281+9G>C	rs370400523	0.00024
NM_002739.5(PRKCG):c.711G>T (p.Glu237Asp)	rs116236420	0.00021
NM_002739.5(PRKCG):c.822-14C>T	rs367639661	0.00013
NM_002739.5(PRKCG):c.*84C>A	rs995740073	0.00010
NM_002739.5(PRKCG):c.940-3C>T	rs377593245	0.00008
NM_002739.5(PRKCG):c.1730C>T (p.Ser577Leu)	rs551805527	0.00006
NM_002739.5(PRKCG):c.441C>T (p.Pro147=)	rs764546467	0.00005
NM_002739.5(PRKCG):c.*48G>A	rs775600229	0.00001
NM_002739.5(PRKCG):c.*59dup	rs144706041

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