ClinVar Miner

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

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Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_006073.4(TRDN):c.1367A>G (p.Gln456Arg) rs200243235 0.00128
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.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.17C>T (p.Ala6Val) rs764897557 0.00001
NM_006073.4(TRDN):c.990A>G (p.Lys330=) rs941068115 0.00001
NM_006073.4(TRDN):c.1369+3dup rs537388823
NM_006073.4(TRDN):c.155T>A (p.Leu52Gln) rs1554258798
NM_006073.4(TRDN):c.2126C>A (p.Ala709Glu) rs876658032
NM_006073.4(TRDN):c.604_610+47del rs1554251571

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