List of variants in gene TRDN reported as benign for catecholaminergic polymorphic ventricular tachycardia 5

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.601C>G (p.Leu201Val)	rs6902416	0.84721
NM_006073.4(TRDN):c.484+41C>T	rs12198167	0.56890
NM_006073.4(TRDN):c.383C>G (p.Thr128Ser)	rs9490809	0.50546
NM_006073.4(TRDN):c.2051-19G>A	rs7754205	0.42872
NM_006073.4(TRDN):c.1188A>G (p.Lys396=)	rs6901953	0.35392
NM_006073.4(TRDN):c.1370-11C>A	rs9401658	0.16989
NM_006073.4(TRDN):c.1620A>G (p.Ile540Met)	rs7771303	0.01556
NM_006073.4(TRDN):c.1096G>A (p.Ala366Thr)	rs35047281	0.01253
NM_006073.4(TRDN):c.1016G>A (p.Ser339Asn)	rs35766971	0.01214
NM_006073.4(TRDN):c.403G>A (p.Glu135Lys)	rs192289289	0.00900
NM_006073.4(TRDN):c.1871-15G>A	rs59935057	0.00724
NM_006073.4(TRDN):c.430C>T (p.His144Tyr)	rs79182520	0.00232
NM_006073.4(TRDN):c.1313T>A (p.Ile438Asn)	rs2873479
NM_006073.4(TRDN):c.1313T>G (p.Ile438Ser)	rs2873479
NM_006073.4(TRDN):c.233-14_233-13del	rs66509682
NM_006073.4(TRDN):c.497AAAAAG[1] (p.166EK[1])	rs148596612

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