List of variants in gene PNPO reported as likely benign by Ambry Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_018129.4(PNPO):c.777T>C (p.Leu259=)	rs142461702	0.00007
NM_018129.4(PNPO):c.306C>T (p.Phe102=)	rs796052866	0.00003
NM_018129.4(PNPO):c.438G>A (p.Val146=)	rs766799976	0.00003
NM_018129.4(PNPO):c.727T>C (p.Leu243=)	rs773871270	0.00003
NM_018129.4(PNPO):c.767A>G (p.Tyr256Cys)	rs148784343	0.00003
NM_018129.4(PNPO):c.16C>A (p.Arg6=)	rs765997859	0.00002

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