List of variants reported as likely pathogenic for catecholaminergic polymorphic ventricular tachycardia 5

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.1282C>T (p.Arg428Ter)	rs202219343	0.00016
NM_006073.4(TRDN):c.1420+1G>T	rs1375657667	0.00003
NM_006073.4(TRDN):c.1050del (p.Glu351fs)	rs753514580
NM_006073.4(TRDN):c.1051+1G>A	rs535908547
NM_006073.4(TRDN):c.1233_1234dup (p.Lys412fs)	rs778198100
NM_006073.4(TRDN):c.1471+1G>A
NM_006073.4(TRDN):c.1553del (p.Lys518fs)
NM_006073.4(TRDN):c.1558G>T (p.Glu520Ter)
NM_006073.4(TRDN):c.1806del (p.Gly603fs)	rs1381728472
NM_006073.4(TRDN):c.391+1G>A	rs2114436209
NM_006073.4(TRDN):c.424+1G>T
NM_006073.4(TRDN):c.531del (p.Glu178fs)	rs1432170970
NM_006073.4(TRDN):c.568dup (p.Ile190fs)	rs1085307100
NM_006073.4(TRDN):c.991G>T (p.Glu331Ter)

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