List of variants in gene PRPF31 reported as benign by Dept Of Ophthalmology, Nagoya University

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_015629.4(PRPF31):c.735C>T (p.Pro245=)	rs11556769	0.08507
NM_015629.4(PRPF31):c.1467C>T (p.Val489=)	rs62144168	0.08162
NM_015629.4(PRPF31):c.1230A>G (p.Thr410=)	rs34154455	0.01460
NM_015629.4(PRPF31):c.1098G>C (p.Leu366=)	rs201201131	0.00044
NM_015629.4(PRPF31):c.414G>A (p.Thr138=)	rs374852494	0.00019
NM_015629.4(PRPF31):c.1158C>T (p.Asp386=)	rs147295591	0.00012
NM_015629.4(PRPF31):c.1320C>T (p.Thr440=)	rs117456605	0.00012
NM_015629.4(PRPF31):c.138T>C (p.Asp46=)	rs76251057	0.00011
NM_015629.4(PRPF31):c.510C>T (p.Thr170=)	rs145699524	0.00011
NM_015629.4(PRPF31):c.1206G>A (p.Ser402=)	rs147663541	0.00009
NM_015629.4(PRPF31):c.1239C>T (p.Asn413=)	rs371720691	0.00008
NM_015629.4(PRPF31):c.251T>C (p.Val84Ala)	rs369049017	0.00005
NM_015629.4(PRPF31):c.1170G>A (p.Glu390=)	rs1212810383

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