ClinVar Miner

List of variants in gene TRAPPC9 reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_001160372.4(TRAPPC9):c.2742C>T (p.Thr914=) rs28710457 0.01086
NM_001160372.4(TRAPPC9):c.456C>T (p.Ile152=) rs61740786 0.00921
NM_001160372.4(TRAPPC9):c.1458C>T (p.Phe486=) rs34179337 0.00827
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_031466.8(TRAPPC9):c.-108A>G rs144686266 0.00305
NM_001160372.4(TRAPPC9):c.588T>C (p.His196=) rs61736350 0.00284
NM_001160372.4(TRAPPC9):c.3291C>T (p.Ser1097=) rs148857575 0.00222
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.1164C>T (p.Tyr388=) rs148976893 0.00136
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.1233C>T (p.Ala411=) rs142390632 0.00067
NM_001160372.4(TRAPPC9):c.3078A>G (p.Pro1026=) rs144039420 0.00063
NM_001160372.4(TRAPPC9):c.3175G>A (p.Ala1059Thr) rs150200902 0.00056
NM_001160372.4(TRAPPC9):c.192G>A (p.Glu64=) rs376133075 0.00043
NM_001160372.4(TRAPPC9):c.2796C>T (p.Ala932=) rs145607512 0.00038
NM_001160372.4(TRAPPC9):c.1809G>A (p.Leu603=) rs146235874 0.00029
NM_001160372.4(TRAPPC9):c.1564G>A (p.Ala522Thr) rs148453804 0.00026
NM_001160372.4(TRAPPC9):c.3168G>A (p.Gly1056=) rs138778665 0.00025
NM_001160372.4(TRAPPC9):c.2772C>T (p.Ser924=) rs143221169 0.00024
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.3438G>A (p.Ala1146=) rs574908324 0.00019
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.3114C>T (p.Gly1038=) rs374300007 0.00014
NM_001160372.4(TRAPPC9):c.198C>T (p.Asn66=) rs142627115 0.00013
NM_001160372.4(TRAPPC9):c.543G>A (p.Pro181=) rs149504969 0.00012
NM_001160372.4(TRAPPC9):c.1311C>T (p.Pro437=) rs3735804 0.00011
NM_001160372.4(TRAPPC9):c.1980C>T (p.Asn660=) rs146730222 0.00011
NM_001160372.4(TRAPPC9):c.1245C>T (p.Cys415=) rs563677377 0.00009
NM_001160372.4(TRAPPC9):c.2775C>T (p.Ser925=) rs547773428 0.00009
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.1881C>T (p.Phe627=) rs774534679 0.00004
NM_001160372.4(TRAPPC9):c.2037G>A (p.Pro679=) rs371880751 0.00004
NM_001160372.4(TRAPPC9):c.1830G>A (p.Pro610=) rs368998062 0.00003
NM_001160372.4(TRAPPC9):c.3288G>A (p.Pro1096=) rs570688248 0.00003
NM_001160372.4(TRAPPC9):c.6C>T (p.Ser2=) rs565904872 0.00003
NM_001160372.4(TRAPPC9):c.2988G>A (p.Glu996=) rs142048892 0.00002
NM_001160372.4(TRAPPC9):c.1296C>T (p.Leu432=) rs760260908 0.00001
NM_001160372.4(TRAPPC9):c.1866C>T (p.Thr622=) rs761031472 0.00001
NM_001160372.4(TRAPPC9):c.2196G>A (p.Gln732=) rs764694089 0.00001
NM_001160372.4(TRAPPC9):c.73A>G (p.Ile25Val) rs571468082 0.00001
NM_031466.8(TRAPPC9):c.-106G>A rs755131283 0.00001
NM_001160372.4(TRAPPC9):c.1041G>A (p.Ala347=)
NM_001160372.4(TRAPPC9):c.1326G>A (p.Ser442=) rs145960296
NM_001160372.4(TRAPPC9):c.1434C>T (p.Ala478=)
NM_001160372.4(TRAPPC9):c.1437C>G (p.Leu479=)
NM_001160372.4(TRAPPC9):c.1533G>T (p.Thr511=)
NM_001160372.4(TRAPPC9):c.1632A>G (p.Lys544=)
NM_001160372.4(TRAPPC9):c.2166A>G (p.Val722=)
NM_001160372.4(TRAPPC9):c.2520C>A (p.Pro840=)
NM_001160372.4(TRAPPC9):c.2539G>A (p.Asp847Asn)
NM_001160372.4(TRAPPC9):c.2571C>T (p.Val857=) rs142325146
NM_001160372.4(TRAPPC9):c.2673C>T (p.Thr891=)
NM_001160372.4(TRAPPC9):c.3147C>T (p.Asn1049=) rs1563769230
NM_001160372.4(TRAPPC9):c.3240C>T (p.Thr1080=)
NM_001160372.4(TRAPPC9):c.3276C>T (p.Asp1092=)
NM_001160372.4(TRAPPC9):c.3420C>T (p.His1140=)
NM_001160372.4(TRAPPC9):c.912C>T (p.Asn304=)
NM_031466.8(TRAPPC9):c.-16G>A

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