ClinVar Miner

List of variants in gene CEP78 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001330691.3(CEP78):c.901A>G (p.Met301Val)	rs200072743	0.00046
NM_001330691.3(CEP78):c.613A>G (p.Met205Val)	rs199972008	0.00006
NM_001330691.3(CEP78):c.680C>T (p.Ala227Val)	rs368402315	0.00005

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