ClinVar Miner

List of variants in gene TRIO reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_007118.4(TRIO):c.2570A>G (p.Asn857Ser) rs199976501 0.00022
NM_007118.4(TRIO):c.7780G>A (p.Ala2594Thr) rs759385450 0.00005
NM_007118.4(TRIO):c.8626C>T (p.Arg2876Cys) rs755026998 0.00004
NM_007118.4(TRIO):c.4146G>A (p.Met1382Ile) rs372498676 0.00003
NM_007118.4(TRIO):c.2340C>G (p.Ile780Met) rs1312892908 0.00002
NM_007118.4(TRIO):c.1682G>A (p.Arg561Gln) rs772006621 0.00001
NM_007118.4(TRIO):c.2465C>T (p.Thr822Met) rs772357380 0.00001
NM_007118.4(TRIO):c.5377G>T (p.Val1793Leu) rs746360543 0.00001
NM_007118.4(TRIO):c.777A>C (p.Glu259Asp) rs1415644561 0.00001
NM_007118.4(TRIO):c.7853T>A (p.Ile2618Asn) rs750714090 0.00001
NM_007118.4(TRIO):c.7978C>T (p.Arg2660Trp) rs748596743 0.00001
NM_007118.4(TRIO):c.8501G>A (p.Arg2834His) rs1219411556 0.00001
NM_007118.4(TRIO):c.9258A>C (p.Lys3086Asn) rs778010546 0.00001
NM_007118.4(TRIO):c.1024C>A (p.Leu342Met)
NM_007118.4(TRIO):c.1411G>C (p.Val471Leu)
NM_007118.4(TRIO):c.1559G>C (p.Ser520Thr)
NM_007118.4(TRIO):c.1681C>T (p.Arg561Trp)
NM_007118.4(TRIO):c.1703T>G (p.Leu568Arg) rs1739412011
NM_007118.4(TRIO):c.1796C>G (p.Ser599Cys)
NM_007118.4(TRIO):c.2243C>A (p.Thr748Asn)
NM_007118.4(TRIO):c.2786T>C (p.Met929Thr)
NM_007118.4(TRIO):c.3021C>G (p.Leu1007=)
NM_007118.4(TRIO):c.3286C>T (p.Pro1096Ser) rs866655659
NM_007118.4(TRIO):c.3414G>C (p.Gln1138His)
NM_007118.4(TRIO):c.3470A>G (p.Asn1157Ser)
NM_007118.4(TRIO):c.3802A>G (p.Ile1268Val)
NM_007118.4(TRIO):c.3935G>A (p.Arg1312Gln)
NM_007118.4(TRIO):c.4108G>A (p.Gly1370Arg)
NM_007118.4(TRIO):c.521G>C (p.Ser174Thr) rs1736499897
NM_007118.4(TRIO):c.5368G>A (p.Asp1790Asn) rs1753772282
NM_007118.4(TRIO):c.551T>G (p.Val184Gly)
NM_007118.4(TRIO):c.5541CTC[2] (p.Ser1850del) rs2126507060
NM_007118.4(TRIO):c.560A>G (p.Glu187Gly) rs1736835991
NM_007118.4(TRIO):c.5658G>A (p.Gln1886=)
NM_007118.4(TRIO):c.5932G>A (p.Val1978Met)
NM_007118.4(TRIO):c.6412G>A (p.Val2138Ile) rs1561540197
NM_007118.4(TRIO):c.6449G>A (p.Arg2150Gln) rs182423419
NM_007118.4(TRIO):c.6877GGC[2] (p.Gly2295_Gly2298del)
NM_007118.4(TRIO):c.6900_6908dup (p.Gly2304_Gly2305insSerGlyGly)
NM_007118.4(TRIO):c.6998C>T (p.Thr2333Met)
NM_007118.4(TRIO):c.7049C>A (p.Pro2350His)
NM_007118.4(TRIO):c.7051G>A (p.Val2351Met)
NM_007118.4(TRIO):c.7135C>T (p.Pro2379Ser)
NM_007118.4(TRIO):c.7137_7148dup (p.Pro2383_Glu2384insGlyAlaAlaPro)
NM_007118.4(TRIO):c.7432C>G (p.Pro2478Ala)
NM_007118.4(TRIO):c.7477C>G (p.Pro2493Ala) rs759022594
NM_007118.4(TRIO):c.7480G>A (p.Ala2494Thr)
NM_007118.4(TRIO):c.7487G>A (p.Arg2496Gln) rs375694147
NM_007118.4(TRIO):c.7595C>T (p.Ala2532Val) rs1400453441
NM_007118.4(TRIO):c.7600G>A (p.Glu2534Lys) rs1579806969
NM_007118.4(TRIO):c.7666A>G (p.Met2556Val)
NM_007118.4(TRIO):c.7688C>T (p.Thr2563Met) rs751663099
NM_007118.4(TRIO):c.8008G>C (p.Val2670Leu)
NM_007118.4(TRIO):c.8019+5G>T
NM_007118.4(TRIO):c.8540T>A (p.Leu2847His) rs2126708999
NM_007118.4(TRIO):c.8680G>A (p.Ala2894Thr)
NM_007118.4(TRIO):c.8711G>T (p.Arg2904Leu) rs182365882
NM_007118.4(TRIO):c.9251G>A (p.Ser3084Asn)
NM_007118.4(TRIO):c.968A>G (p.Gln323Arg) rs777932649

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