List of variants in gene PROKR2 reported 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
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_144773.4(PROKR2):c.151G>A (p.Ala51Thr)	rs144994507	0.00303
NM_144773.4(PROKR2):c.518T>G (p.Leu173Arg)	rs74315416	0.00220
NM_144773.4(PROKR2):c.1005G>A (p.Thr335=)	rs150381386	0.00190
NM_144773.4(PROKR2):c.991G>A (p.Val331Met)	rs117106081	0.00088
NM_144773.4(PROKR2):c.375C>T (p.His125=)	rs148596437	0.00076
NM_144773.4(PROKR2):c.390C>T (p.Ser130=)	rs144778137	0.00054
NM_144773.4(PROKR2):c.1058G>A (p.Arg353His)	rs576243101	0.00006
NM_144773.4(PROKR2):c.349C>T (p.Arg117Trp)	rs142008002	0.00006
NM_144773.4(PROKR2):c.403C>T (p.Arg135Cys)	rs149396342	0.00003
NM_144773.4(PROKR2):c.1000G>T (p.Val334Leu)
NM_144773.4(PROKR2):c.254G>A (p.Arg85His)	rs74315418
NM_144773.4(PROKR2):c.271C>T (p.Leu91Phe)
NM_144773.4(PROKR2):c.472G>A (p.Val158Ile)
NM_144773.4(PROKR2):c.510C>T (p.Ala170=)
NM_144773.4(PROKR2):c.58del (p.His20fs)	rs587777834
NM_144773.4(PROKR2):c.819G>T (p.Thr273=)

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