List of variants in gene PTS reported as uncertain significance 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000317.3(PTS):c.338A>G (p.Tyr113Cys)	rs762894736	0.00003
NM_000317.3(PTS):c.370G>T (p.Val124Leu)	rs150726932	0.00003
NM_000317.3(PTS):c.186G>A (p.Glu62=)	rs189051075	0.00001
NM_000317.3(PTS):c.379C>G (p.Leu127Val)	rs1859971515	0.00001
NM_000317.3(PTS):c.130A>G (p.Asn44Asp)	rs2496564225
NM_000317.3(PTS):c.179A>C (p.His60Pro)
NM_000317.3(PTS):c.194C>T (p.Pro65Leu)	rs2496567536

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