List of variants in gene GNPTG reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_032520.5(GNPTG):c.233+35C>T	rs144929410	0.00165
NM_032520.5(GNPTG):c.814A>G (p.Arg272Gly)	rs8062558	0.00128
NM_032520.5(GNPTG):c.183C>T (p.Pro61=)	rs140264422	0.00061
NM_032520.5(GNPTG):c.684C>G (p.Thr228=)	rs150965148	0.00060
NM_032520.5(GNPTG):c.903G>A (p.Leu301=)	rs141807632	0.00043
NM_032520.5(GNPTG):c.603C>T (p.Thr201=)	rs146171435	0.00038
NM_032520.5(GNPTG):c.502G>A (p.Val168Ile)	rs190614894	0.00014
NM_032520.5(GNPTG):c.411+15G>A	rs375386449	0.00006
NM_032520.5(GNPTG):c.233+9A>T	rs1596612776
NM_032520.5(GNPTG):c.339C>T (p.Ile113=)	rs147048228
NM_032520.5(GNPTG):c.610-28G>C

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