ClinVar Miner

Variants in gene TRAPPC9 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 39
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HGVS dbSNP gnomAD frequency
NM_001160372.4(TRAPPC9):c.1869C>T (p.Ser623=) rs117685875 0.01001
NM_001160372.4(TRAPPC9):c.1458C>T (p.Phe486=) rs34179337 0.00827
NM_001160372.4(TRAPPC9):c.2797G>A (p.Gly933Ser) rs114949291 0.00641
NM_001160372.4(TRAPPC9):c.3163G>A (p.Val1055Ile) rs35578974 0.00512
NM_001160372.4(TRAPPC9):c.3249C>T (p.Phe1083=) rs112551069 0.00501
NM_001160372.4(TRAPPC9):c.588T>C (p.His196=) rs61736350 0.00284
NM_001160372.4(TRAPPC9):c.1407C>T (p.Tyr469=) rs117632905 0.00151
NM_001160372.4(TRAPPC9):c.3421G>A (p.Val1141Met) rs140157207 0.00147
NM_001160372.4(TRAPPC9):c.1164C>T (p.Tyr388=) rs148976893 0.00136
NM_001160372.4(TRAPPC9):c.3149G>A (p.Arg1050Gln) rs111768745 0.00103
NM_001160372.4(TRAPPC9):c.159C>T (p.Leu53=) rs112997540 0.00089
NM_001160372.4(TRAPPC9):c.3414T>G (p.Ser1138Arg) rs147127279 0.00089
NM_001160372.4(TRAPPC9):c.3241G>A (p.Val1081Ile) rs141067069 0.00078
NM_001160372.4(TRAPPC9):c.263C>T (p.Ser88Leu) rs139631202 0.00072
NM_031466.8(TRAPPC9):c.-11+6C>T rs376367358 0.00066
NM_001160372.4(TRAPPC9):c.3175G>A (p.Ala1059Thr) rs150200902 0.00056
NM_001160372.4(TRAPPC9):c.2796C>T (p.Ala932=) rs145607512 0.00038
NM_001160372.4(TRAPPC9):c.3356G>A (p.Arg1119Gln) rs145503551 0.00034
NM_001160372.4(TRAPPC9):c.1809G>A (p.Leu603=) rs146235874 0.00029
NM_001160372.4(TRAPPC9):c.3411C>A (p.Pro1137=) rs373979305 0.00022
NM_001160372.4(TRAPPC9):c.370A>G (p.Ile124Val) rs117688394 0.00022
NM_001160372.4(TRAPPC9):c.2981G>C (p.Ser994Thr) rs377114410 0.00016
NM_001160372.4(TRAPPC9):c.3136C>T (p.Arg1046Trp) rs376617920 0.00015
NM_001160372.4(TRAPPC9):c.1194C>T (p.Ile398=) rs587780484 0.00011
NM_031466.8(TRAPPC9):c.-24G>A rs370984854 0.00009
NM_001160372.4(TRAPPC9):c.2245C>T (p.Leu749=) rs375545861 0.00006
NM_001160372.4(TRAPPC9):c.3055+10C>T rs571622542 0.00006
NM_001160372.4(TRAPPC9):c.2037G>A (p.Pro679=) rs371880751 0.00004
NM_001160372.4(TRAPPC9):c.2704C>T (p.Arg902Trp) rs370626310 0.00004
NM_001160372.4(TRAPPC9):c.2793C>T (p.His931=) rs886062722 0.00004
NM_001160372.4(TRAPPC9):c.1768+7C>T rs587780485 0.00003
NM_001160372.4(TRAPPC9):c.3288G>A (p.Pro1096=) rs570688248 0.00003
NM_001160372.4(TRAPPC9):c.2988G>A (p.Glu996=) rs142048892 0.00002
NM_001160372.4(TRAPPC9):c.1560C>T (p.Pro520=) rs886062724 0.00001
NM_001160372.4(TRAPPC9):c.3148C>T (p.Arg1050Trp) rs563050274 0.00001
NM_001160372.4(TRAPPC9):c.1326G>A (p.Ser442=) rs145960296
NM_001160372.4(TRAPPC9):c.2279-11del rs758850777
NM_001160372.4(TRAPPC9):c.2475G>A (p.Arg825=) rs756688439
NM_001160372.4(TRAPPC9):c.269A>G (p.Lys90Arg) rs550423753

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