ClinVar Miner

List of variants in gene PRPF31 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_015629.4(PRPF31):c.935C>T (p.Thr312Ile)	rs144322132	0.00008
NM_015629.4(PRPF31):c.1140C>T (p.Phe380=)	rs1411083098	0.00001

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