ClinVar Miner

List of variants in gene PNPO reported by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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_018129.4(PNPO):c.98A>T (p.Asp33Val)	rs370243877	0.00012
NM_018129.4(PNPO):c.479C>A (p.Ser160Tyr)
NM_018129.4(PNPO):c.481C>T (p.Arg161Cys)	rs146027425

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