List of variants in gene PRPF31 reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_015629.4(PRPF31):c.*197G>C	rs886054620	0.00013
NM_015629.4(PRPF31):c.632G>A (p.Arg211Gln)	rs201806410	0.00012
NM_015629.4(PRPF31):c.1268C>T (p.Thr423Met)	rs753277924	0.00002
NM_015629.4(PRPF31):c.1243G>A (p.Ala415Thr)	rs1222805069	0.00001

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