ClinVar Miner

Variants in gene TRAPPC9 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 42
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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.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_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.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_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.543G>A (p.Pro181=) rs149504969 0.00012
NM_031466.8(TRAPPC9):c.-73G>C rs767996463 0.00005
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.1326G>A (p.Ser442=) rs145960296
NM_001160372.4(TRAPPC9):c.1353C>T (p.Gly451=)
NM_001160372.4(TRAPPC9):c.3087C>T (p.Arg1029=) rs561829257
NM_001160372.4(TRAPPC9):c.3225C>T (p.Tyr1075=) rs58740567

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