List of variants in gene NAPG reported as uncertain significance

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_003826.3(NAPG):c.929G>A (p.Gly310Glu)	rs201175120	0.00042
NM_003826.3(NAPG):c.283G>A (p.Val95Ile)	rs201039776	0.00023
NM_003826.3(NAPG):c.764A>G (p.Asn255Ser)	rs371701856	0.00023
NM_003826.3(NAPG):c.452G>A (p.Arg151Gln)	rs200300448	0.00011
NM_003826.3(NAPG):c.349G>A (p.Ala117Thr)	rs376946681	0.00002
NM_003826.3(NAPG):c.202A>G (p.Asn68Asp)	rs746984473	0.00001
NM_003826.3(NAPG):c.427G>C (p.Val143Leu)	rs965850649	0.00001
NM_003826.3(NAPG):c.212T>G (p.Leu71Arg)	rs2510174263
NM_003826.3(NAPG):c.265C>G (p.Gln89Glu)
NM_003826.3(NAPG):c.332C>A (p.Pro111Gln)	rs2510176930
NM_003826.3(NAPG):c.446G>A (p.Arg149His)
NM_003826.3(NAPG):c.497G>A (p.Arg166Gln)	rs749319093
NM_003826.3(NAPG):c.518C>T (p.Ala173Val)	rs956039626
NM_003826.3(NAPG):c.521C>T (p.Ala174Val)
NM_003826.3(NAPG):c.543_545del (p.Lys181del)	rs756804159
NM_003826.3(NAPG):c.547A>G (p.Ile183Val)
NM_003826.3(NAPG):c.595G>A (p.Ala199Thr)	rs1158807232
NM_003826.3(NAPG):c.667A>G (p.Ile223Val)
NM_003826.3(NAPG):c.721G>A (p.Gly241Ser)
NM_003826.3(NAPG):c.878A>G (p.Asp293Gly)

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