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

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 38

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HGVS	dbSNP	gnomAD frequency
NM_002739.5(PRKCG):c.*427T>C	rs886054615	0.00334
NM_002739.5(PRKCG):c.*622C>G	rs1032868211	0.00046
NM_002739.5(PRKCG):c.*550C>T	rs778703745	0.00035
NM_002739.5(PRKCG):c.1747G>A (p.Val583Met)	rs143513754	0.00014
NM_002739.5(PRKCG):c.234C>T (p.His78=)	rs143456958	0.00010
NM_002739.5(PRKCG):c.*426C>T	rs1002891475	0.00006
NM_002739.5(PRKCG):c.1730C>T (p.Ser577Leu)	rs551805527	0.00006
NM_002739.5(PRKCG):c.*184C>T	rs764816557	0.00005
NM_002739.5(PRKCG):c.*481T>C	rs886054616	0.00003
NM_002739.5(PRKCG):c.1665C>T (p.Phe555=)	rs556667568	0.00003
NM_002739.5(PRKCG):c.1904C>T (p.Pro635Leu)	rs1360248213	0.00003
NM_002739.5(PRKCG):c.-233C>T	rs752173466	0.00002
NM_002739.5(PRKCG):c.1382C>T (p.Ala461Val)	rs751774653	0.00002
NM_002739.5(PRKCG):c.529+11G>T	rs886054612	0.00002
NM_002739.5(PRKCG):c.*360G>C	rs886054614	0.00001
NM_002739.5(PRKCG):c.*415G>C	rs2068821858	0.00001
NM_002739.5(PRKCG):c.-169G>C	rs777064041	0.00001
NM_002739.5(PRKCG):c.1282-14G>A	rs1017029385	0.00001
NM_002739.5(PRKCG):c.1883C>T (p.Pro628Leu)	rs1303074743	0.00001
NM_002739.5(PRKCG):c.1900C>T (p.Arg634Cys)	rs980400591	0.00001
NM_002739.5(PRKCG):c.1906-10T>C	rs575700585	0.00001
NM_002739.5(PRKCG):c.1960C>T (p.Leu654=)	rs753906154	0.00001
NM_002739.5(PRKCG):c.2086G>A (p.Val696Ile)	rs751824637	0.00001
NM_002739.5(PRKCG):c.520C>G (p.His174Asp)	rs777612378	0.00001
NM_002739.5(PRKCG):c.637C>A (p.Arg213=)	rs750289253	0.00001
NM_002739.5(PRKCG):c.712C>T (p.Arg238Cys)	rs771732555	0.00001
NM_002739.5(PRKCG):c.*39C>T	rs776490487
NM_002739.5(PRKCG):c.1210G>A (p.Ala404Thr)	rs769292201
NM_002739.5(PRKCG):c.1232G>C (p.Gly411Ala)
NM_002739.5(PRKCG):c.1451A>T (p.Asp484Val)
NM_002739.5(PRKCG):c.1571C>G (p.Pro524Arg)
NM_002739.5(PRKCG):c.1712C>G (p.Thr571Ser)
NM_002739.5(PRKCG):c.1764+8C>T	rs756397908
NM_002739.5(PRKCG):c.1962G>C (p.Leu654=)	rs868833808
NM_002739.5(PRKCG):c.347A>G (p.His116Arg)	rs2068657131
NM_002739.5(PRKCG):c.475G>A (p.Gly159Arg)	rs866406014
NM_002739.5(PRKCG):c.686+300C>G	rs2068681112
NM_002739.5(PRKCG):c.715C>T (p.Arg239Trp)	rs1471641294

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