ClinVar Miner

List of variants in gene TRAPPC9 reported as uncertain significance by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 106
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HGVS dbSNP gnomAD frequency
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.3149G>A (p.Arg1050Gln) rs111768745 0.00103
NM_001160372.4(TRAPPC9):c.3414T>G (p.Ser1138Arg) rs147127279 0.00089
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.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.2681G>A (p.Ser894Asn) rs34181302 0.00029
NM_001160372.4(TRAPPC9):c.2077G>A (p.Ala693Thr) rs147044768 0.00026
NM_001160372.4(TRAPPC9):c.140G>A (p.Arg47Gln) rs147182402 0.00024
NM_001160372.4(TRAPPC9):c.1628T>C (p.Val543Ala) rs200886297 0.00024
NM_001160372.4(TRAPPC9):c.3211G>A (p.Gly1071Ser) rs200963473 0.00014
NM_031466.8(TRAPPC9):c.-74C>A rs139214686 0.00011
NM_001160372.4(TRAPPC9):c.2882C>T (p.Ala961Val) rs769398594 0.00010
NM_001160372.4(TRAPPC9):c.940G>A (p.Ala314Thr) rs762765901 0.00010
NM_001160372.4(TRAPPC9):c.136G>A (p.Val46Met) rs201233141 0.00009
NM_031466.8(TRAPPC9):c.-24G>A rs370984854 0.00009
NM_001160372.4(TRAPPC9):c.3220A>G (p.Asn1074Asp) rs762135474 0.00007
NM_001160372.4(TRAPPC9):c.1196G>A (p.Gly399Asp) rs376272150 0.00006
NM_001160372.4(TRAPPC9):c.2827G>C (p.Asp943His) rs144046998 0.00006
NM_001160372.4(TRAPPC9):c.1352-5C>T rs376013888 0.00004
NM_001160372.4(TRAPPC9):c.2704C>T (p.Arg902Trp) rs370626310 0.00004
NM_001160372.4(TRAPPC9):c.2811-4G>A rs374826041 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.3088G>A (p.Glu1030Lys) rs766920866 0.00004
NM_001160372.4(TRAPPC9):c.76G>A (p.Val26Ile) rs376505164 0.00004
NM_001160372.4(TRAPPC9):c.3013C>A (p.Gln1005Lys) rs913893905 0.00003
NM_001160372.4(TRAPPC9):c.805C>T (p.Arg269Trp) rs779077167 0.00003
NM_001160372.4(TRAPPC9):c.2705G>A (p.Arg902Gln) rs768169759 0.00002
NM_001160372.4(TRAPPC9):c.902A>G (p.Asn301Ser) rs779620347 0.00002
NM_001160372.4(TRAPPC9):c.1184A>G (p.Tyr395Cys) rs370310318 0.00001
NM_001160372.4(TRAPPC9):c.1524G>C (p.Glu508Asp) rs754444715 0.00001
NM_001160372.4(TRAPPC9):c.1870G>A (p.Gly624Arg) rs772315237 0.00001
NM_001160372.4(TRAPPC9):c.1988A>G (p.His663Arg) rs200557642 0.00001
NM_001160372.4(TRAPPC9):c.2622G>T (p.Arg874Ser) rs202169819 0.00001
NM_001160372.4(TRAPPC9):c.3158G>A (p.Arg1053His) rs369074996 0.00001
NM_001160372.4(TRAPPC9):c.52G>A (p.Val18Met) rs759083867 0.00001
NM_001160372.4(TRAPPC9):c.-4C>A rs1284713164
NM_001160372.4(TRAPPC9):c.1005C>G (p.Ser335Arg)
NM_001160372.4(TRAPPC9):c.1013A>T (p.Lys338Met)
NM_001160372.4(TRAPPC9):c.1069A>G (p.Ile357Val)
NM_001160372.4(TRAPPC9):c.1109A>G (p.Asn370Ser)
NM_001160372.4(TRAPPC9):c.1170C>G (p.Ile390Met)
NM_001160372.4(TRAPPC9):c.1226G>A (p.Arg409His)
NM_001160372.4(TRAPPC9):c.1234G>T (p.Ala412Ser)
NM_001160372.4(TRAPPC9):c.1262C>T (p.Ala421Val)
NM_001160372.4(TRAPPC9):c.1337A>G (p.Lys446Arg)
NM_001160372.4(TRAPPC9):c.1352-4G>A
NM_001160372.4(TRAPPC9):c.1355C>A (p.Thr452Lys)
NM_001160372.4(TRAPPC9):c.1355C>T (p.Thr452Met)
NM_001160372.4(TRAPPC9):c.1538A>G (p.Lys513Arg)
NM_001160372.4(TRAPPC9):c.1618G>A (p.Val540Ile)
NM_001160372.4(TRAPPC9):c.1642C>A (p.Leu548Ile)
NM_001160372.4(TRAPPC9):c.1654C>T (p.Leu552Phe)
NM_001160372.4(TRAPPC9):c.1732G>A (p.Ala578Thr)
NM_001160372.4(TRAPPC9):c.1911G>A (p.Pro637=) rs148353187
NM_001160372.4(TRAPPC9):c.1942G>A (p.Val648Ile)
NM_001160372.4(TRAPPC9):c.1958C>T (p.Thr653Met)
NM_001160372.4(TRAPPC9):c.1981G>A (p.Gly661Ser)
NM_001160372.4(TRAPPC9):c.1994C>T (p.Thr665Met)
NM_001160372.4(TRAPPC9):c.2020T>A (p.Leu674Met)
NM_001160372.4(TRAPPC9):c.2032C>G (p.Leu678Val) rs1563915700
NM_001160372.4(TRAPPC9):c.2144G>A (p.Gly715Asp)
NM_001160372.4(TRAPPC9):c.2192G>A (p.Ser731Asn)
NM_001160372.4(TRAPPC9):c.2283A>C (p.Lys761Asn)
NM_001160372.4(TRAPPC9):c.2307G>T (p.Trp769Cys)
NM_001160372.4(TRAPPC9):c.2482G>A (p.Val828Ile)
NM_001160372.4(TRAPPC9):c.2485C>T (p.Arg829Trp)
NM_001160372.4(TRAPPC9):c.2521G>A (p.Glu841Lys)
NM_001160372.4(TRAPPC9):c.2525G>A (p.Ser842Asn)
NM_001160372.4(TRAPPC9):c.2584T>C (p.Tyr862His)
NM_001160372.4(TRAPPC9):c.265G>A (p.Ala89Thr)
NM_001160372.4(TRAPPC9):c.2675G>C (p.Arg892Pro)
NM_001160372.4(TRAPPC9):c.2690C>A (p.Pro897Gln)
NM_001160372.4(TRAPPC9):c.271G>A (p.Asp91Asn)
NM_001160372.4(TRAPPC9):c.2728G>A (p.Val910Ile)
NM_001160372.4(TRAPPC9):c.2743G>A (p.Glu915Lys)
NM_001160372.4(TRAPPC9):c.2800G>A (p.Glu934Lys)
NM_001160372.4(TRAPPC9):c.2852C>T (p.Pro951Leu)
NM_001160372.4(TRAPPC9):c.3041C>T (p.Ala1014Val)
NM_001160372.4(TRAPPC9):c.3067G>T (p.Asp1023Tyr)
NM_001160372.4(TRAPPC9):c.3124C>T (p.Arg1042Cys)
NM_001160372.4(TRAPPC9):c.3225C>A (p.Tyr1075Ter) rs58740567
NM_001160372.4(TRAPPC9):c.3249C>G (p.Phe1083Leu)
NM_001160372.4(TRAPPC9):c.3257C>T (p.Ser1086Phe)
NM_001160372.4(TRAPPC9):c.3292G>A (p.Gly1098Ser)
NM_001160372.4(TRAPPC9):c.420C>G (p.Asp140Glu)
NM_001160372.4(TRAPPC9):c.457G>A (p.Glu153Lys)
NM_001160372.4(TRAPPC9):c.598C>T (p.Arg200Trp)
NM_001160372.4(TRAPPC9):c.616C>T (p.Arg206Trp)
NM_001160372.4(TRAPPC9):c.761T>G (p.Val254Gly)
NM_001160372.4(TRAPPC9):c.775C>T (p.Pro259Ser)
NM_001160372.4(TRAPPC9):c.838G>A (p.Ala280Thr)
NM_001160372.4(TRAPPC9):c.938G>T (p.Arg313Leu)
NM_001160372.4(TRAPPC9):c.949T>A (p.Cys317Ser)
NM_031466.8(TRAPPC9):c.-134G>T rs1564040977
NM_031466.8(TRAPPC9):c.-162C>A
NM_031466.8(TRAPPC9):c.-212G>C
NM_031466.8(TRAPPC9):c.-231C>T
NM_031466.8(TRAPPC9):c.-68C>T
NM_031466.8(TRAPPC9):c.-69C>T

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