List of variants in gene CENPE reported as uncertain significance by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001813.3(CENPE):c.4791A>C (p.Arg1597Ser)	rs61751594	0.00360
NM_001813.3(CENPE):c.3749C>G (p.Thr1250Ser)	rs114698062	0.00217
NM_001813.3(CENPE):c.6928A>G (p.Ile2310Val)	rs111281600	0.00175
NM_001813.3(CENPE):c.6203G>C (p.Arg2068Thr)	rs148969710	0.00094
NM_001813.3(CENPE):c.4273G>A (p.Gly1425Arg)	rs116330917	0.00075
NM_001813.3(CENPE):c.7294C>T (p.Leu2432Phe)	rs142518565	0.00074
NM_001813.3(CENPE):c.7886G>A (p.Arg2629Gln)	rs141321114	0.00024
NM_001813.3(CENPE):c.304C>T (p.His102Tyr)	rs758681737	0.00010
NM_001813.3(CENPE):c.4997A>G (p.Glu1666Gly)	rs138953137	0.00006
NM_001813.3(CENPE):c.3435T>A (p.Asn1145Lys)	rs374126277	0.00004
NM_001813.3(CENPE):c.7202A>G (p.Glu2401Gly)	rs762068581	0.00004
NM_001813.3(CENPE):c.739G>A (p.Ala247Thr)	rs138379874	0.00004
NM_001813.3(CENPE):c.5137A>G (p.Ile1713Val)	rs921819934	0.00002
NM_001813.3(CENPE):c.5563C>T (p.Gln1855Ter)	rs1214805862
NM_001813.3(CENPE):c.7173T>G (p.His2391Gln)	rs1195686700

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