List of variants reported as likely pathogenic for Catecholaminergic polymorphic ventricular tachycardia 5 by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.176C>T (p.Thr59Met)	rs397515459	0.00001
NM_006073.4(TRDN):c.541G>T (p.Glu181Ter)	rs1198103383	0.00001
NM_006073.4(TRDN):c.326del (p.Leu109fs)	rs2534485312
NM_006073.4(TRDN):c.383del (p.Thr128fs)
NM_006073.4(TRDN):c.483del (p.Val162fs)	rs1780193710
NM_006073.4(TRDN):c.601_610+45delinsG	rs2534332866
NM_006073.4(TRDN):c.680_681del (p.Gln227fs)

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