List of variants in gene PRX reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_181882.3(PRX):c.2145T>A (p.Cys715Ter)	rs104894707	0.00006
NM_181882.3(PRX):c.1090C>T (p.Arg364Ter)	rs144183238	0.00005
NM_181882.3(PRX):c.2857C>T (p.Arg953Ter)	rs104894714	0.00003
NM_181882.3(PRX):c.589G>T (p.Glu197Ter)	rs753857146	0.00003
NM_181882.3(PRX):c.1102C>T (p.Arg368Ter)	rs104894715	0.00001
NM_181882.3(PRX):c.1390C>T (p.Arg464Ter)	rs574861276	0.00001
NM_181882.3(PRX):c.3611del (p.Leu1204fs)	rs776887800	0.00001
NM_181882.3(PRX):c.2602del (p.Gln868fs)	rs1303287747
NM_181882.3(PRX):c.2787del (p.Lys930fs)	rs754521978
NM_181882.3(PRX):c.2853dup (p.Gly952fs)	rs1568704829
NM_181882.3(PRX):c.3286_3356del (p.Ile1096fs)	rs1555800610
NM_181882.3(PRX):c.4050del (p.Ser1351fs)	rs766124869
NM_181882.3(PRX):c.586C>T (p.Arg196Ter)	rs104894706
NM_181882.3(PRX):c.627del (p.Ala210fs)	rs1599656507

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