List of variants in gene PRX reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_181882.3(PRX):c.1483G>C (p.Glu495Gln)	rs146789340	0.01068
NM_181882.3(PRX):c.1216G>A (p.Ala406Thr)	rs117336941	0.00456
NM_181882.3(PRX):c.3846G>A (p.Ser1282=)	rs143289108	0.00288
NM_181882.3(PRX):c.445G>A (p.Ala149Thr)	rs142436391	0.00193
NM_181882.3(PRX):c.3373G>A (p.Gly1125Ser)	rs148939995	0.00191
NM_181882.3(PRX):c.2254G>A (p.Glu752Lys)	rs147587689	0.00185
NM_181882.3(PRX):c.3947C>T (p.Ala1316Val)	rs142762689	0.00138
NM_181882.3(PRX):c.1574T>C (p.Val525Ala)	rs149715830	0.00136
NM_181882.3(PRX):c.823C>A (p.Leu275Ile)	rs200033507	0.00108
NM_181882.3(PRX):c.2548C>G (p.Pro850Ala)	rs141686828	0.00078
NM_181882.3(PRX):c.966G>T (p.Val322=)	rs139544245	0.00042
NM_181882.3(PRX):c.3549C>T (p.Tyr1183=)	rs367876251	0.00017
NM_181882.3(PRX):c.1222C>T (p.Pro408Ser)	rs150244426	0.00004
NM_181882.3(PRX):c.2715C>A (p.Thr905=)	rs188765166	0.00004
NM_181882.3(PRX):c.3423G>A (p.Ala1141=)	rs370800046	0.00002
NM_181882.3(PRX):c.1749T>G (p.Pro583=)	rs1234792110	0.00001
NM_181882.3(PRX):c.2804A>C (p.Lys935Thr)	rs1179595016	0.00001
NM_181882.3(PRX):c.825C>T (p.Leu275=)	rs753268672	0.00001
NM_181882.3(PRX):c.834G>A (p.Pro278=)	rs759984063	0.00001
NM_181882.3(PRX):c.1863G>A (p.Val621=)
NM_181882.3(PRX):c.1944T>C (p.Ala648=)
NM_181882.3(PRX):c.1953T>C (p.Asp651=)
NM_181882.3(PRX):c.2859A>G (p.Arg953=)
NM_181882.3(PRX):c.2913G>T (p.Val971=)	rs1599652077
NM_181882.3(PRX):c.3606T>G (p.Gly1202=)
NM_181882.3(PRX):c.876C>G (p.Val292=)

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