List of variants in gene KPRP reported as uncertain significance for carcinoma

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_001025231.3(KPRP):c.743G>A (p.Arg248His)	rs193921023	0.00001
NM_001025231.3(KPRP):c.825T>A (p.Phe275Leu)	rs193920890

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