List of variants in gene PRX reported by Baylor Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_181882.3(PRX):c.500G>C (p.Arg167Pro)	rs757322355	0.00019
NM_181882.3(PRX):c.718C>T (p.Arg240Trp)	rs199863083	0.00011
NM_181882.3(PRX):c.4118G>A (p.Arg1373Gln)	rs763294661	0.00010
NM_181882.3(PRX):c.1546C>T (p.Arg516Trp)	rs144305922	0.00008
NM_181882.3(PRX):c.4307G>A (p.Arg1436Gln)	rs368827070	0.00006
NM_181882.3(PRX):c.4317C>T (p.Ser1439=)	rs372280596	0.00006
NM_181882.3(PRX):c.2790G>C (p.Lys930Asn)	rs758614032	0.00003
NM_181882.3(PRX):c.2857C>T (p.Arg953Ter)	rs104894714	0.00003
NM_181882.3(PRX):c.3919C>T (p.Arg1307Trp)	rs752593001	0.00002
NM_181882.3(PRX):c.1184C>T (p.Thr395Ile)	rs1273087776	0.00001
NM_181882.3(PRX):c.2719C>T (p.Gln907Ter)	rs2079426412
NM_181882.3(PRX):c.4330G>C (p.Glu1444Gln)	rs2079403438

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