ClinVar Miner

List of variants in gene TRDN reported as uncertain significance for Catecholaminergic polymorphic ventricular tachycardia

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Gene type:
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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_006073.4(TRDN):c.1864A>G (p.Ser622Gly) rs577376276 0.00005
NM_006073.4(TRDN):c.1975+5G>T rs899940538 0.00002
NM_006073.4(TRDN):c.1018G>A (p.Glu340Lys) rs778821180 0.00001
NC_000006.11:g.(?_123536484)_(123959238_?)dup
NC_000006.11:g.(?_123539737)_(123957930_?)dup
NC_000006.11:g.(?_123581598)_(123581802_?)del
NC_000006.11:g.(?_123581747)_(123581793_?)del
NC_000006.11:g.(?_123586443)_(123588916_?)dup
NC_000006.11:g.(?_123818328)_(123825056_?)del
NC_000006.11:g.(?_123851641)_(123851720_?)del
NC_000006.12:g.(?_123260612)_(123260638_?)del
NC_000006.12:g.(?_123337609)_(123439013_?)dup
NC_000006.12:g.(?_123547330)_(123548622_?)del
NM_006073.4(TRDN):c.*1456CA[3] rs764560250
NM_006073.4(TRDN):c.1052-9C>T rs765883002
NM_006073.4(TRDN):c.109A>T (p.Thr37Ser) rs1554258810
NM_006073.4(TRDN):c.1720G>A (p.Ala574Thr) rs866787639
NM_006073.4(TRDN):c.233-13del rs66509682
NM_006073.4(TRDN):c.233-15_233-13del rs66509682
NM_006073.4(TRDN):c.425-4_425-3insLINE1
NM_006073.4(TRDN):c.932-6C>A rs886061033

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