List of variants in gene PRPF31 reported as benign by Illumina Laboratory Services, Illumina

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_015629.4(PRPF31):c.-9+14=	rs4806711	0.17623
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.564G>A (p.Glu188=)	rs1058572	0.02280
NM_015629.4(PRPF31):c.239-13C>T	rs113691122	0.02250
NM_015629.4(PRPF31):c.1230A>G (p.Thr410=)	rs34154455	0.01460
NM_015629.4(PRPF31):c.1302A>G (p.Val434=)	rs35230170	0.01449
NM_015629.4(PRPF31):c.*19G>A	rs116685547	0.01038
NM_015629.4(PRPF31):c.1416G>A (p.Val472=)	rs145958840	0.00763
NM_015629.4(PRPF31):c.420+7G>A	rs143717956	0.00723
NM_015629.4(PRPF31):c.138T>C (p.Asp46=)	rs76251057	0.00011
NM_015629.4(PRPF31):c.*46G>A	rs368621219	0.00001
NM_015629.4(PRPF31):c.1147-9=	rs655240

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