List of variants studied for Epilepsy, familial focal, with variable foci 3 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001077350.3(NPRL3):c.997G>A (p.Val333Ile)	rs367664536	0.00012
NM_001077350.3(NPRL3):c.1375_1376dup (p.Ser460fs)	rs886037960
NM_001077350.3(NPRL3):c.1557C>G (p.Tyr519Ter)	rs2141895094
NM_001077350.3(NPRL3):c.189-1G>A	rs1900184374
NM_001077350.3(NPRL3):c.393+4_393+7del	rs757371554

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