ClinVar Miner

List of variants in gene TRAPPC9 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 49
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HGVS dbSNP gnomAD frequency
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.2799= (p.Gly933=) rs2614718 0.08065
NM_001160372.4(TRAPPC9):c.2742C>T (p.Thr914=) rs28710457 0.01086
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.3249C>T (p.Phe1083=) rs112551069 0.00501
NM_001160372.4(TRAPPC9):c.3291C>T (p.Ser1097=) rs148857575 0.00222
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.3241G>A (p.Val1081Ile) rs141067069 0.00078
NM_001160372.4(TRAPPC9):c.263C>T (p.Ser88Leu) rs139631202 0.00072
NM_001160372.4(TRAPPC9):c.1233C>T (p.Ala411=) rs142390632 0.00067
NM_001160372.4(TRAPPC9):c.2671A>C (p.Thr891Pro) rs562249191 0.00066
NM_001160372.4(TRAPPC9):c.3078A>G (p.Pro1026=) rs144039420 0.00063
NM_001160372.4(TRAPPC9):c.2871G>A (p.Lys957=) rs188700138 0.00045
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_031466.8(TRAPPC9):c.-256G>A rs144294636 0.00016
NM_001160372.4(TRAPPC9):c.3114C>T (p.Gly1038=) rs374300007 0.00014
NM_001160372.4(TRAPPC9):c.543G>A (p.Pro181=) rs149504969 0.00012
NM_001160372.4(TRAPPC9):c.1194C>T (p.Ile398=) rs587780484 0.00011
NM_001160372.4(TRAPPC9):c.1678T>C (p.Leu560=) rs139848315 0.00010
NM_001160372.4(TRAPPC9):c.2901G>C (p.Glu967Asp) rs139074311 0.00010
NM_001160372.4(TRAPPC9):c.2811-4G>A rs374826041 0.00004
NM_001160372.4(TRAPPC9):c.1693G>A (p.Val565Met) rs551407866 0.00002
NM_001160372.4(TRAPPC9):c.687G>A (p.Ser229=) rs776317177 0.00001
NM_001160372.4(TRAPPC9):c.1045del (p.Ile349fs)
NM_001160372.4(TRAPPC9):c.108G>A (p.Lys36=)
NM_001160372.4(TRAPPC9):c.1281C>T (p.Ala427=) rs545979845
NM_001160372.4(TRAPPC9):c.1353C>T (p.Gly451=)
NM_001160372.4(TRAPPC9):c.1521A>G (p.Leu507=)
NM_001160372.4(TRAPPC9):c.1736A>C (p.His579Pro)
NM_001160372.4(TRAPPC9):c.2166A>G (p.Val722=)
NM_001160372.4(TRAPPC9):c.2305T>C (p.Trp769Arg)
NM_001160372.4(TRAPPC9):c.252A>C (p.Thr84=)
NM_001160372.4(TRAPPC9):c.2664A>G (p.Val888=)
NM_001160372.4(TRAPPC9):c.2727T>C (p.Asp909=)
NM_001160372.4(TRAPPC9):c.274_280del (p.Trp92fs) rs1554689964
NM_001160372.4(TRAPPC9):c.3051G>A (p.Gln1017=)
NM_031466.8(TRAPPC9):c.-129_-109dup rs367682297
NM_031466.8(TRAPPC9):c.-157A>C

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