ClinVar Miner

List of variants in gene TRAPPC9 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 101
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001160372.4(TRAPPC9):c.2799T>C (p.Gly933=) rs2614718 0.91935
NM_001160372.4(TRAPPC9):c.730+299A>G rs13257015 0.80358
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.730+190A>C rs13264229 0.42471
NM_001160372.4(TRAPPC9):c.730+235C>T rs13281374 0.42275
NM_001160372.4(TRAPPC9):c.860-86G>A rs6998221 0.41793
NM_001160372.4(TRAPPC9):c.2279-310G>T rs12334515 0.39856
NM_001160372.4(TRAPPC9):c.1768+284T>C rs7828853 0.34546
NM_001160372.4(TRAPPC9):c.2114+303C>T rs73366986 0.32395
NM_001160372.4(TRAPPC9):c.1768+82T>C rs12156047 0.30909
NM_001160372.4(TRAPPC9):c.2811-155G>A rs1551806 0.28655
NM_001160372.4(TRAPPC9):c.1134+21A>G rs3779658 0.27421
NM_001160372.4(TRAPPC9):c.2279-301G>A rs11166966 0.22792
NM_001160372.4(TRAPPC9):c.1692C>T (p.Asn564=) rs12549048 0.22639
NM_001160372.4(TRAPPC9):c.3056-281T>C rs199225 0.22533
NM_001160372.4(TRAPPC9):c.*104C>T rs199226 0.19615
NM_001160372.4(TRAPPC9):c.2279-183_2279-182del rs140935423 0.13556
NM_001160372.4(TRAPPC9):c.1854+89T>A rs62527544 0.11975
NM_001160372.4(TRAPPC9):c.2700-190C>T rs7821102 0.11021
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.2810+206C>T rs6989296 0.09497
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.-10-77C>T rs73713134 0.08878
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.3280-146C>A rs58933385 0.04803
NM_001160372.4(TRAPPC9):c.2278+265C>T rs73714850 0.04144
NM_001160372.4(TRAPPC9):c.2278+247C>G rs73714851 0.04140
NM_001160372.4(TRAPPC9):c.2278+275C>T rs73714849 0.04112
NM_001160372.4(TRAPPC9):c.1134+47C>T rs75617021 0.03814
NM_001160372.4(TRAPPC9):c.1768+257C>G rs113072129 0.03624
NM_001160372.4(TRAPPC9):c.3280-292C>T rs112885631 0.03460
NM_001160372.4(TRAPPC9):c.1769-122A>T rs77369667 0.03310
NM_001160372.4(TRAPPC9):c.1855-93dup rs111465816 0.03010
NM_001160372.4(TRAPPC9):c.2557-146G>A rs73725374 0.02979
NM_001160372.4(TRAPPC9):c.2279-178T>C rs62527491 0.02955
NM_001160372.4(TRAPPC9):c.585-305A>G rs75631105 0.02882
NM_001160372.4(TRAPPC9):c.3279+4C>T rs79877357 0.02434
NM_001160372.4(TRAPPC9):c.2964+120T>G rs78093868 0.02297
NM_001160372.4(TRAPPC9):c.3055+18A>G rs111467460 0.02216
NM_001160372.4(TRAPPC9):c.2811-326C>T rs115291100 0.02119
NM_001160372.4(TRAPPC9):c.2556+38T>C rs114869664 0.01882
NM_001160372.4(TRAPPC9):c.1982-20A>C rs74414386 0.01477
NM_001160372.4(TRAPPC9):c.2742C>T (p.Thr914=) rs28710457 0.01086
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.584+19C>T rs143903438 0.00701
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.7G>A (p.Val3Ile) rs76033442 0.00489
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.2871G>A (p.Lys957=) rs188700138 0.00045
NM_031466.8(TRAPPC9):c.-135A>G rs148523016 0.00037
NM_001160372.4(TRAPPC9):c.1809G>A (p.Leu603=) rs146235874 0.00029
NM_001160372.4(TRAPPC9):c.2556+11A>G rs201489589 0.00029
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.1215G>A (p.Ala405=) rs148641824 0.00011
NM_031466.8(TRAPPC9):c.-73G>C rs767996463 0.00005
NM_001160372.4(TRAPPC9):c.2079G>A (p.Ala693=) rs200235924 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.1693G>A (p.Val565Met) rs551407866 0.00002
NM_001160372.4(TRAPPC9):c.1866C>T (p.Thr622=) rs761031472 0.00001
NM_001160372.4(TRAPPC9):c.*532G>A rs187594197
NM_001160372.4(TRAPPC9):c.-10-26C>T rs9657463
NM_001160372.4(TRAPPC9):c.1134+226GTTT[3] rs3837157
NM_001160372.4(TRAPPC9):c.1326G>A (p.Ser442=) rs145960296
NM_001160372.4(TRAPPC9):c.1353C>T (p.Gly451=)
NM_001160372.4(TRAPPC9):c.1981+94A>G rs6999767
NM_001160372.4(TRAPPC9):c.2114+60dup rs368141971
NM_001160372.4(TRAPPC9):c.2115-112C>T rs73366966
NM_001160372.4(TRAPPC9):c.2557-13del rs111869504
NM_001160372.4(TRAPPC9):c.2557-13dup rs111869504
NM_001160372.4(TRAPPC9):c.2557-36GT[7] rs147021256
NM_001160372.4(TRAPPC9):c.2700-12del rs1447678589
NM_001160372.4(TRAPPC9):c.2700-3C>T rs1837438136
NM_001160372.4(TRAPPC9):c.2810+17C>A rs374999568
NM_001160372.4(TRAPPC9):c.3087C>T (p.Arg1029=) rs561829257
NM_001160372.4(TRAPPC9):c.3225C>T (p.Tyr1075=) rs58740567
NM_001160372.4(TRAPPC9):c.731-31_731-11del rs11267571
NM_001160372.4(TRAPPC9):c.859+142del rs371009615
NM_031466.8(TRAPPC9):c.-11+123_-11+132del rs143157829
NM_031466.8(TRAPPC9):c.-129_-109dup rs367682297

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.