ClinVar Miner

List of variants reported as benign for catecholaminergic polymorphic ventricular tachycardia 5 by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Included ClinVar conditions (2):
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ClinVar version:
Total variants: 8
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HGVS dbSNP gnomAD frequency
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.497AAAAAG[1] (p.166EK[1]) rs148596612

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