ClinVar Miner

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

Included ClinVar conditions (17):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
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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+1457C>T rs9490795 0.56990
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.1186+16C>T rs3813328 0.33405
NM_006073.4(TRDN):c.1257C>A (p.Asp419Glu) rs17737379 0.17356
NM_006073.4(TRDN):c.1370-11C>A rs9401658 0.16989
NM_006073.4(TRDN):c.1211T>G (p.Val404Gly) rs28494009 0.16504
NM_006073.4(TRDN):c.1408C>A (p.Leu470Met) rs6569336 0.09024
NM_006073.4(TRDN):c.1805-6C>T rs201544606 0.03259
NM_006073.4(TRDN):c.1105+5G>A rs41284430 0.03253
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.274G>A (p.Val92Ile) rs34808221 0.00711
NM_006073.4(TRDN):c.1538-13T>G rs55704802 0.00651
NM_006073.4(TRDN):c.1567+19T>C rs182813107 0.00459
NM_006073.4(TRDN):c.1721-4A>G rs60743141 0.00430
NM_006073.4(TRDN):c.430C>T (p.His144Tyr) rs79182520 0.00232
NM_006073.4(TRDN):c.932-4C>G rs77768246 0.00098
NM_006073.4(TRDN):c.1472-12G>A rs375364108 0.00036
NM_006073.4(TRDN):c.367G>A (p.Asp123Asn) rs201021891 0.00036
NM_006073.4(TRDN):c.2050+16G>A rs543899749 0.00003
NM_006073.4(TRDN):c.1052-10dup
NM_006073.4(TRDN):c.1105+13del
NM_006073.4(TRDN):c.1135+17dup
NM_006073.4(TRDN):c.1187-2A>G rs578024729
NM_006073.4(TRDN):c.1220-19del
NM_006073.4(TRDN):c.1220-19dup rs750105897
NM_006073.4(TRDN):c.1220-20_1220-19del
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.1369+3dup rs537388823
NM_006073.4(TRDN):c.1511-13del rs768721605
NM_006073.4(TRDN):c.1511-13dup
NM_006073.4(TRDN):c.1598-6dup rs147062785
NM_006073.4(TRDN):c.1784-10dup rs1776904446
NM_006073.4(TRDN):c.1784-17del rs750605412
NM_006073.4(TRDN):c.1784-17dup
NM_006073.4(TRDN):c.1805-21dup rs11373802
NM_006073.4(TRDN):c.1906+14del
NM_006073.4(TRDN):c.1975+9G>A rs111276785
NM_006073.4(TRDN):c.2015-10del
NM_006073.4(TRDN):c.2015-10dup
NM_006073.4(TRDN):c.233-14_233-13del rs66509682
NM_006073.4(TRDN):c.497AAAAAG[1] (p.166EK[1]) rs148596612
NM_006073.4(TRDN):c.931+18del rs201431159
NM_006073.4(TRDN):c.931+18dup rs201431159

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