ClinVar Miner

List of variants in gene TRAPPC9 studied for not specified

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Gene type:
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Total variants: 122
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HGVS dbSNP gnomAD frequency
NM_001160372.4(TRAPPC9):c.2799T>C (p.Gly933=) rs2614718 0.91935
NM_001160372.4(TRAPPC9):c.2557-13T>A rs9792174 0.57247
NM_001160372.4(TRAPPC9):c.207T>C (p.Gly69=) rs3735801 0.55959
NM_001160372.4(TRAPPC9):c.288T>C (p.Phe96=) rs3735802 0.55845
NM_001160372.4(TRAPPC9):c.411C>T (p.Asn137=) rs3735803 0.45974
NM_001160372.4(TRAPPC9):c.1692C>T (p.Asn564=) rs12549048 0.22639
NM_001160372.4(TRAPPC9):c.2292C>T (p.Gly764=) rs11166965 0.10684
NM_001160372.4(TRAPPC9):c.2431+7G>A rs11166964 0.10663
NM_001160372.4(TRAPPC9):c.399T>C (p.Ala133=) rs61739560 0.08885
NM_001160372.4(TRAPPC9):c.555G>A (p.Lys185=) rs57593250 0.08881
NM_001160372.4(TRAPPC9):c.357G>A (p.Gly119=) rs34457678 0.08878
NM_001160372.4(TRAPPC9):c.2799= (p.Gly933=) rs2614718 0.08065
NM_001160372.4(TRAPPC9):c.3279+4C>T rs79877357 0.02434
NM_031466.8(TRAPPC9):c.-11+10G>A rs117206975 0.01054
NM_001160372.4(TRAPPC9):c.1869C>T (p.Ser623=) rs117685875 0.01001
NM_001160372.4(TRAPPC9):c.456C>T (p.Ile152=) rs61740786 0.00921
NM_001160372.4(TRAPPC9):c.414C>T (p.Tyr138=) rs115986561 0.00912
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.3390A>C (p.Pro1130=) rs143396124 0.00333
NM_001160372.4(TRAPPC9):c.588T>C (p.His196=) rs61736350 0.00284
NM_001160372.4(TRAPPC9):c.3069C>T (p.Asp1023=) rs144383785 0.00187
NM_001160372.4(TRAPPC9):c.1407C>T (p.Tyr469=) rs117632905 0.00151
NM_001160372.4(TRAPPC9):c.3012C>T (p.Asn1004=) rs148805943 0.00151
NM_001160372.4(TRAPPC9):c.3421G>A (p.Val1141Met) rs140157207 0.00147
NM_001160372.4(TRAPPC9):c.3157C>T (p.Arg1053Cys) rs147499593 0.00144
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_001160372.4(TRAPPC9):c.2671A>C (p.Thr891Pro) rs562249191 0.00066
NM_031466.8(TRAPPC9):c.-11+6C>T rs376367358 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.2658G>A (p.Pro886=) rs150252117 0.00044
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.2796C>T (p.Ala932=) rs145607512 0.00038
NM_031466.8(TRAPPC9):c.-135A>G rs148523016 0.00037
NM_001160372.4(TRAPPC9):c.3237C>T (p.Asp1079=) rs144880704 0.00035
NM_001160372.4(TRAPPC9):c.3356G>A (p.Arg1119Gln) rs145503551 0.00034
NM_001160372.4(TRAPPC9):c.564A>G (p.Val188=) rs150743393 0.00032
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.3168G>A (p.Gly1056=) rs138778665 0.00025
NM_001160372.4(TRAPPC9):c.140G>A (p.Arg47Gln) rs147182402 0.00024
NM_001160372.4(TRAPPC9):c.2772C>T (p.Ser924=) rs143221169 0.00024
NM_001160372.4(TRAPPC9):c.384G>A (p.Pro128=) rs140509196 0.00023
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.2981G>C (p.Ser994Thr) rs377114410 0.00016
NM_031466.8(TRAPPC9):c.-256G>A rs144294636 0.00016
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.543G>A (p.Pro181=) rs149504969 0.00012
NM_001160372.4(TRAPPC9):c.1980C>T (p.Asn660=) rs146730222 0.00011
NM_001160372.4(TRAPPC9):c.1678T>C (p.Leu560=) rs139848315 0.00010
NM_001160372.4(TRAPPC9):c.2882C>T (p.Ala961Val) rs769398594 0.00010
NM_001160372.4(TRAPPC9):c.1245C>T (p.Cys415=) rs563677377 0.00009
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.2076C>T (p.Pro692=) rs761179684 0.00006
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.1263G>A (p.Ala421=) rs113690180 0.00005
NM_031466.8(TRAPPC9):c.-73G>C rs767996463 0.00005
NM_001160372.4(TRAPPC9):c.2037G>A (p.Pro679=) rs371880751 0.00004
NM_001160372.4(TRAPPC9):c.2811-5C>T rs534788967 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.1693G>A (p.Val565Met) rs551407866 0.00002
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.1731C>T (p.Ile577=) rs756282844 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.2361G>A (p.Thr787=) rs145964915 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.687G>A (p.Ser229=) rs776317177 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.1533G>A (p.Thr511=) rs750274973
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.3225C>T (p.Tyr1075=) 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
NM_031466.8(TRAPPC9):c.-244C>T rs1334808447

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