ClinVar Miner

List of variants in gene TRAPPC9 reported as uncertain significance for not specified

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Gene type:
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Total variants: 68
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HGVS dbSNP gnomAD frequency
NM_001160372.4(TRAPPC9):c.588T>C (p.His196=) rs61736350 0.00284
NM_001160372.4(TRAPPC9):c.3421G>A (p.Val1141Met) rs140157207 0.00147
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.3241G>A (p.Val1081Ile) rs141067069 0.00078
NM_001160372.4(TRAPPC9):c.263C>T (p.Ser88Leu) rs139631202 0.00072
NM_001160372.4(TRAPPC9):c.2671A>C (p.Thr891Pro) rs562249191 0.00066
NM_001160372.4(TRAPPC9):c.2794G>A (p.Ala932Thr) rs148909256 0.00058
NM_001160372.4(TRAPPC9):c.1019C>T (p.Ala340Val) rs143778652 0.00056
NM_001160372.4(TRAPPC9):c.3175G>A (p.Ala1059Thr) rs150200902 0.00056
NM_001160372.4(TRAPPC9):c.853C>T (p.Arg285Trp) rs141441030 0.00045
NM_001160372.4(TRAPPC9):c.44C>T (p.Thr15Met) rs142839408 0.00043
NM_001160372.4(TRAPPC9):c.814C>A (p.Gln272Lys) rs144569575 0.00040
NM_001160372.4(TRAPPC9):c.3356G>A (p.Arg1119Gln) rs145503551 0.00034
NM_001160372.4(TRAPPC9):c.2681G>A (p.Ser894Asn) rs34181302 0.00029
NM_001160372.4(TRAPPC9):c.1564G>A (p.Ala522Thr) rs148453804 0.00026
NM_001160372.4(TRAPPC9):c.1898C>T (p.Ala633Val) rs375300224 0.00025
NM_001160372.4(TRAPPC9):c.140G>A (p.Arg47Gln) rs147182402 0.00024
NM_001160372.4(TRAPPC9):c.3411C>A (p.Pro1137=) rs373979305 0.00022
NM_001160372.4(TRAPPC9):c.82G>A (p.Glu28Lys) rs151056818 0.00020
NM_001160372.4(TRAPPC9):c.3136C>T (p.Arg1046Trp) rs376617920 0.00015
NM_001160372.4(TRAPPC9):c.3211G>A (p.Gly1071Ser) rs200963473 0.00014
NM_001160372.4(TRAPPC9):c.2882C>T (p.Ala961Val) rs769398594 0.00010
NM_001160372.4(TRAPPC9):c.2921G>A (p.Arg974Gln) rs562020701 0.00009
NM_001160372.4(TRAPPC9):c.3220A>G (p.Asn1074Asp) rs762135474 0.00007
NM_001160372.4(TRAPPC9):c.2258C>T (p.Ser753Leu) rs766369011 0.00006
NM_001160372.4(TRAPPC9):c.1177G>A (p.Glu393Lys) rs145782440 0.00005
NM_001160372.4(TRAPPC9):c.2037G>A (p.Pro679=) rs371880751 0.00004
NM_001160372.4(TRAPPC9):c.3056A>C (p.Asp1019Ala) rs755371528 0.00004
NM_001160372.4(TRAPPC9):c.1078C>T (p.Arg360Trp) rs374392590 0.00003
NM_001160372.4(TRAPPC9):c.1357C>T (p.His453Tyr) rs534194766 0.00003
NM_001160372.4(TRAPPC9):c.1385G>A (p.Arg462His) rs746266971 0.00003
NM_001160372.4(TRAPPC9):c.1420A>G (p.Met474Val) rs752614138 0.00003
NM_001160372.4(TRAPPC9):c.3278C>T (p.Ala1093Val) rs750167029 0.00003
NM_001160372.4(TRAPPC9):c.805C>T (p.Arg269Trp) rs779077167 0.00003
NM_001160372.4(TRAPPC9):c.2341C>A (p.Gln781Lys) rs758925630 0.00002
NM_001160372.4(TRAPPC9):c.1524G>C (p.Glu508Asp) rs754444715 0.00001
NM_001160372.4(TRAPPC9):c.1603A>T (p.Thr535Ser) rs756125925 0.00001
NM_001160372.4(TRAPPC9):c.1948G>A (p.Val650Ile) rs770244296 0.00001
NM_001160372.4(TRAPPC9):c.1982-9C>T rs758604818 0.00001
NM_001160372.4(TRAPPC9):c.2343G>T (p.Gln781His) rs748576558 0.00001
NM_001160372.4(TRAPPC9):c.2597C>T (p.Pro866Leu) rs199948844 0.00001
NM_001160372.4(TRAPPC9):c.2662G>A (p.Val888Ile) rs1397394319 0.00001
NM_001160372.4(TRAPPC9):c.3148C>T (p.Arg1050Trp) rs563050274 0.00001
NM_001160372.4(TRAPPC9):c.3217C>T (p.His1073Tyr) rs1459705932 0.00001
NM_001160372.4(TRAPPC9):c.3364G>A (p.Glu1122Lys) rs767963216 0.00001
NM_001160372.4(TRAPPC9):c.937C>T (p.Arg313Cys) rs201224878 0.00001
NM_031466.8(TRAPPC9):c.-203G>C rs797046049 0.00001
NM_031466.8(TRAPPC9):c.-58G>A rs886062730 0.00001
GRCh37/hg19 8q24.3(chr8:141016802-141086121)
GRCh37/hg19 8q24.3(chr8:141016802-141446902)
GRCh37/hg19 8q24.3(chr8:141286569-141519946)
NM_001160372.4(TRAPPC9):c.1173C>T (p.Leu391=) rs547129477
NM_001160372.4(TRAPPC9):c.1294C>A (p.Leu432Ile) rs1554676260
NM_001160372.4(TRAPPC9):c.1326G>A (p.Ser442=) rs145960296
NM_001160372.4(TRAPPC9):c.1634T>G (p.Leu545Arg) rs2131826248
NM_001160372.4(TRAPPC9):c.1745G>C (p.Gly582Ala) rs797046048
NM_001160372.4(TRAPPC9):c.269A>G (p.Lys90Arg) rs550423753
NM_001160372.4(TRAPPC9):c.26G>A (p.Cys9Tyr) rs932408437
NM_001160372.4(TRAPPC9):c.291G>C (p.Glu97Asp) rs1554689955
NM_001160372.4(TRAPPC9):c.2971C>T (p.Leu991=) rs1829987688
NM_001160372.4(TRAPPC9):c.3225C>A (p.Tyr1075Ter) rs58740567
NM_001160372.4(TRAPPC9):c.3292G>C (p.Gly1098Arg) rs536787964
NM_001160372.4(TRAPPC9):c.3325C>A (p.Leu1109Ile) rs371403079
NM_001160372.4(TRAPPC9):c.584G>C (p.Arg195Thr) rs1554689856
NM_001160372.4(TRAPPC9):c.653T>A (p.Met218Lys) rs797046050
NM_001160372.4(TRAPPC9):c.938G>A (p.Arg313His) rs757159552
NM_031466.8(TRAPPC9):c.-219G>A rs750200775

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