ClinVar Miner

List of variants in gene TRAPPC11 reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_021942.6(TRAPPC11):c.931C>G (p.Leu311Val) rs148833310 0.00057
NM_021942.6(TRAPPC11):c.2851+5G>A rs373713956 0.00034
NM_021942.6(TRAPPC11):c.1901A>G (p.Asn634Ser) rs148567547 0.00026
NM_021942.6(TRAPPC11):c.3400T>C (p.Ter1134Arg) rs142222368 0.00021
NM_021942.6(TRAPPC11):c.1277T>C (p.Val426Ala) rs201263451 0.00009
NM_021942.6(TRAPPC11):c.3211G>A (p.Gly1071Ser) rs141588557 0.00007
NM_021942.6(TRAPPC11):c.1058C>G (p.Ala353Gly) rs200078740 0.00006
NM_021942.6(TRAPPC11):c.1530G>T (p.Lys510Asn) rs139154209 0.00006
NM_021942.6(TRAPPC11):c.1745A>G (p.Gln582Arg) rs533474499 0.00006
NM_021942.6(TRAPPC11):c.2234C>A (p.Thr745Lys) rs768000138 0.00004
NM_021942.6(TRAPPC11):c.3194G>A (p.Arg1065Gln) rs567387885 0.00004
NM_021942.6(TRAPPC11):c.3074G>A (p.Arg1025His) rs374203755 0.00003
NM_021942.6(TRAPPC11):c.3215C>T (p.Thr1072Met) rs147061560 0.00003
NM_021942.6(TRAPPC11):c.597T>G (p.Tyr199Ter) rs373475855 0.00003
NM_021942.6(TRAPPC11):c.899A>T (p.Asp300Val) rs768253464 0.00003
NM_021942.6(TRAPPC11):c.130C>T (p.Arg44Trp) rs757210292 0.00002
NM_021942.6(TRAPPC11):c.3062C>T (p.Pro1021Leu) rs371103166 0.00002
NM_021942.6(TRAPPC11):c.1208G>A (p.Ser403Asn) rs761391260 0.00001
NM_021942.6(TRAPPC11):c.1329C>G (p.Phe443Leu) rs368173953 0.00001
NM_021942.6(TRAPPC11):c.1543T>C (p.Tyr515His) rs901204498 0.00001
NM_021942.6(TRAPPC11):c.2087G>A (p.Gly696Glu) rs775381679 0.00001
NM_021942.6(TRAPPC11):c.2560C>A (p.Leu854Ile) rs771646323 0.00001
NM_021942.6(TRAPPC11):c.2708A>G (p.Glu903Gly) rs1398795151 0.00001
NM_021942.6(TRAPPC11):c.3073C>T (p.Arg1025Cys) rs771331017 0.00001
NM_021942.6(TRAPPC11):c.3217G>A (p.Glu1073Lys) rs760646935 0.00001
NM_021942.6(TRAPPC11):c.660+5G>A rs770891745 0.00001
NM_021942.6(TRAPPC11):c.1305T>A (p.Leu435=) rs373944670
NM_021942.6(TRAPPC11):c.1364T>C (p.Leu455Pro) rs2111363123
NM_021942.6(TRAPPC11):c.2032G>A (p.Val678Met) rs2111060987
NM_021942.6(TRAPPC11):c.2530C>T (p.Arg844Cys) rs149626892
NM_021942.6(TRAPPC11):c.2674G>T (p.Val892Phe)
NM_021942.6(TRAPPC11):c.686A>G (p.Lys229Arg)

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