ClinVar Miner

List of variants in gene TRDN reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 47
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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.383C>G (p.Thr128Ser) rs9490809 0.50546
NM_006073.4(TRDN):c.1188A>G (p.Lys396=) rs6901953 0.35392
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.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.1721-4A>G rs60743141 0.00430
NM_006073.4(TRDN):c.430C>T (p.His144Tyr) rs79182520 0.00232
NM_006073.4(TRDN):c.1531C>A (p.Pro511Thr) rs146935076 0.00183
NM_006073.4(TRDN):c.793+61T>C rs572614305 0.00177
NM_006073.4(TRDN):c.1367A>G (p.Gln456Arg) rs200243235 0.00128
NM_006073.4(TRDN):c.932-4C>G rs77768246 0.00098
NM_006073.4(TRDN):c.84C>T (p.Pro28=) rs145992727 0.00070
NM_006073.4(TRDN):c.1895G>A (p.Arg632Lys) rs181571822 0.00044
NM_006073.4(TRDN):c.546G>A (p.Lys182=) rs377594350 0.00042
NM_006073.4(TRDN):c.1193A>T (p.Glu398Val) rs374355537 0.00041
NM_006073.4(TRDN):c.1472-12G>A rs375364108 0.00036
NM_006073.4(TRDN):c.1472-13C>T rs367962513 0.00033
NM_006073.4(TRDN):c.129G>A (p.Thr43=) rs373840513 0.00011
NM_006073.4(TRDN):c.793+27G>A rs189106156 0.00011
NM_006073.4(TRDN):c.125C>T (p.Thr42Met) rs371627659 0.00010
NM_006073.4(TRDN):c.1801C>G (p.Pro601Ala) rs376214235 0.00007
NM_006073.4(TRDN):c.46G>C (p.Val16Leu) rs974343553 0.00003
NM_006073.4(TRDN):c.592A>G (p.Thr198Ala) rs952211002 0.00003
NM_006073.4(TRDN):c.17C>T (p.Ala6Val) rs764897557 0.00001
NM_006073.4(TRDN):c.232+15A>T rs769101414 0.00001
NM_006073.4(TRDN):c.990A>G (p.Lys330=) rs941068115 0.00001
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.1511-14T>C rs1252673540
NM_006073.4(TRDN):c.155T>A (p.Leu52Gln) rs1554258798
NM_006073.4(TRDN):c.1597+10G>A rs150165710
NM_006073.4(TRDN):c.1598-6dup rs147062785
NM_006073.4(TRDN):c.2126C>A (p.Ala709Glu) rs876658032
NM_006073.4(TRDN):c.497AAAAAG[1] (p.166EK[1]) rs148596612
NM_006073.4(TRDN):c.604_610+47del rs1554251571
NM_006073.4(TRDN):c.931+18del rs201431159

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