List of variants in gene CEP135 reported as likely benign 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_025009.5(CEP135):c.2305A>C (p.Ile769Leu)	rs3214045	0.20167
NM_025009.5(CEP135):c.2976C>G (p.Thr992=)	rs35143702	0.02394
NM_025009.5(CEP135):c.3075T>C (p.Asn1025=)	rs61753870	0.02389
NM_025009.5(CEP135):c.1220G>A (p.Ser407Asn)	rs62641664	0.01474
NM_025009.5(CEP135):c.2724A>G (p.Arg908=)	rs113687114	0.01034
NM_025009.5(CEP135):c.1254A>G (p.Arg418=)	rs62641662	0.00274
NM_025009.5(CEP135):c.2065A>G (p.Ile689Val)	rs139407231	0.00252
NM_025009.5(CEP135):c.638T>C (p.Val213Ala)	rs150331261	0.00236
NM_025009.5(CEP135):c.2971A>G (p.Met991Val)	rs115646074	0.00232
NM_025009.5(CEP135):c.2755A>C (p.Arg919=)	rs151170797	0.00202
NM_025009.5(CEP135):c.636A>C (p.Glu212Asp)	rs76941356	0.00181
NM_025009.5(CEP135):c.2398G>C (p.Asp800His)	rs143195447	0.00167
NM_025009.5(CEP135):c.1920G>A (p.Ser640=)	rs375822537	0.00012

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