ClinVar Miner

List of variants in gene TSEN54 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 35
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HGVS dbSNP gnomAD frequency
NM_207346.3(TSEN54):c.1122G>C (p.Arg374=) rs6501820 0.89534
NM_207346.3(TSEN54):c.285+32C>A rs7218675 0.64612
NM_207346.3(TSEN54):c.1310C>T (p.Ala437Val) rs8064529 0.63819
NM_207346.3(TSEN54):c.1041G>C (p.Lys347Asn) rs9911502 0.58492
NM_207346.3(TSEN54):c.114T>G (p.His38Gln) rs8079373 0.19277
NM_207346.3(TSEN54):c.285+3G>A rs8074291 0.19227
NM_207346.3(TSEN54):c.333C>G (p.Arg111=) rs6501818 0.19222
NM_207346.3(TSEN54):c.370-19C>A rs56895494 0.12137
NM_207346.3(TSEN54):c.409A>C (p.Ile137Leu) rs11559205 0.09934
NM_207346.3(TSEN54):c.1166A>C (p.Gln389Pro) rs77247739 0.09564
NM_207346.3(TSEN54):c.521+39C>T rs57636645 0.06538
NM_207346.3(TSEN54):c.624-37A>C rs73998306 0.06523
NM_207346.3(TSEN54):c.1573G>C (p.Gly525Arg) rs11870627 0.05898
NM_207346.3(TSEN54):c.1447C>G (p.Pro483Ala) rs62088470 0.04801
NM_207346.3(TSEN54):c.568G>A (p.Val190Met) rs79508780 0.04141
NM_207346.3(TSEN54):c.222-18C>T rs113255333 0.02242
NM_207346.3(TSEN54):c.1468C>T (p.Arg490Trp) rs144662042 0.01362
NM_207346.3(TSEN54):c.1328C>G (p.Ser443Cys) rs150169668 0.01002
NM_207346.3(TSEN54):c.1167G>C (p.Gln389His) rs369805010 0.00193
NM_207346.3(TSEN54):c.83C>T (p.Ser28Leu) rs201089582 0.00116
NM_207346.3(TSEN54):c.959C>T (p.Pro320Leu) rs189860274 0.00084
NM_207346.3(TSEN54):c.624-31A>G rs191600766 0.00080
NM_207346.3(TSEN54):c.1368C>T (p.Asp456=) rs138560086 0.00075
NM_207346.3(TSEN54):c.222-40C>G rs368933303 0.00071
NM_207346.3(TSEN54):c.692C>T (p.Pro231Leu) rs141249409 0.00070
NM_207346.3(TSEN54):c.468+47A>T rs201404842 0.00068
NM_207346.3(TSEN54):c.767G>A (p.Gly256Asp) rs200683263 0.00061
NM_207346.3(TSEN54):c.624-10C>T rs368876457 0.00008
NM_207346.3(TSEN54):c.1071G>A (p.Ala357=) rs371212469 0.00007
NM_207346.3(TSEN54):c.1430+4C>T rs202109896 0.00004
NM_207346.3(TSEN54):c.720C>T (p.Cys240=) rs372368367 0.00002
NM_207346.3(TSEN54):c.1414C>G (p.Arg472Gly)
NM_207346.3(TSEN54):c.285+30GCCCTCCCT[2] rs58038334
NM_207346.3(TSEN54):c.457C>T (p.Leu153=)
NM_207346.3(TSEN54):c.474C>T (p.Phe158=)

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