ClinVar Miner

List of variants in gene TNFRSF9 studied for not provided

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Gene type:
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Total variants: 159
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HGVS dbSNP gnomAD frequency
NM_001561.6(TNFRSF9):c.30C>T (p.Ala10=) rs1565745 0.01612
NM_001561.6(TNFRSF9):c.84T>C (p.Cys28=) rs61446318 0.01591
NM_001561.6(TNFRSF9):c.527C>A (p.Ala176Asp) rs9657979 0.01021
NM_001561.6(TNFRSF9):c.166G>A (p.Ala56Thr) rs9657963 0.00332
NM_001561.6(TNFRSF9):c.291A>G (p.Ala97=) rs146308127 0.00254
NM_001561.6(TNFRSF9):c.345A>C (p.Lys115Asn) rs9657965 0.00079
NM_001561.6(TNFRSF9):c.501G>A (p.Pro167=) rs148554600 0.00041
NM_001561.6(TNFRSF9):c.506C>T (p.Ala169Val) rs144772280 0.00030
NM_001561.6(TNFRSF9):c.346+11G>A rs371929562 0.00026
NM_001561.6(TNFRSF9):c.401G>A (p.Arg134Gln) rs186372948 0.00014
NM_001561.6(TNFRSF9):c.70T>C (p.Leu24=) rs148398132 0.00012
NM_001561.6(TNFRSF9):c.413+4C>T rs373663685 0.00008
NM_001561.6(TNFRSF9):c.680-12T>A rs543185072 0.00006
NM_001561.6(TNFRSF9):c.722G>A (p.Cys241Tyr) rs752191416 0.00006
NM_001561.6(TNFRSF9):c.500C>T (p.Pro167Leu) rs145966863 0.00005
NM_001561.6(TNFRSF9):c.100+19T>C rs374144124 0.00004
NM_001561.6(TNFRSF9):c.100+1G>A rs754024907 0.00004
NM_001561.6(TNFRSF9):c.209G>A (p.Gly70Asp) rs202220858 0.00004
NM_001561.6(TNFRSF9):c.346+10C>T rs754883091 0.00004
NM_001561.6(TNFRSF9):c.576T>A (p.Leu192=) rs753713618 0.00004
NM_001561.6(TNFRSF9):c.749A>G (p.Glu250Gly) rs776878260 0.00004
NM_001561.6(TNFRSF9):c.265A>C (p.Thr89Pro) rs752678621 0.00003
NM_001561.6(TNFRSF9):c.465C>T (p.Asp155=) rs373859958 0.00003
NM_001561.6(TNFRSF9):c.679C>T (p.Pro227Ser) rs533883433 0.00003
NM_001561.6(TNFRSF9):c.165C>T (p.Ser55=) rs150479025 0.00002
NM_001561.6(TNFRSF9):c.413+8T>C rs780100518 0.00002
NM_001561.6(TNFRSF9):c.63A>G (p.Thr21=) rs748894187 0.00002
NM_001561.6(TNFRSF9):c.643C>T (p.Arg215Trp) rs143524950 0.00002
NM_001561.6(TNFRSF9):c.680-13A>T rs778402646 0.00002
NM_001561.6(TNFRSF9):c.100G>A (p.Gly34Ser) rs201012166 0.00001
NM_001561.6(TNFRSF9):c.13T>G (p.Cys5Gly) rs556537043 0.00001
NM_001561.6(TNFRSF9):c.156T>C (p.Ser52=) rs769441615 0.00001
NM_001561.6(TNFRSF9):c.21C>A (p.Asn7Lys) rs1252718070 0.00001
NM_001561.6(TNFRSF9):c.286G>C (p.Gly96Arg) rs759034075 0.00001
NM_001561.6(TNFRSF9):c.378C>T (p.Asn126=) rs765656918 0.00001
NM_001561.6(TNFRSF9):c.400C>T (p.Arg134Ter) rs771142611 0.00001
NM_001561.6(TNFRSF9):c.452C>T (p.Thr151Met) rs769884031 0.00001
NM_001561.6(TNFRSF9):c.466G>A (p.Val156Met) rs1289916547 0.00001
NM_001561.6(TNFRSF9):c.545-4G>T rs908519580 0.00001
NM_001561.6(TNFRSF9):c.571T>C (p.Phe191Leu) rs758622644 0.00001
NM_001561.6(TNFRSF9):c.588G>A (p.Ser196=) rs376451216 0.00001
NM_001561.6(TNFRSF9):c.626G>A (p.Arg209His) rs1239035274 0.00001
NM_001561.6(TNFRSF9):c.649A>G (p.Arg217Gly) rs780812476 0.00001
NM_001561.6(TNFRSF9):c.707A>G (p.Gln236Arg) rs1024785003 0.00001
NC_000001.10:g.(?_7993202)_(7993376_?)del
NM_001561.6(TNFRSF9):c.100+5G>A
NM_001561.6(TNFRSF9):c.101-3T>A
NM_001561.6(TNFRSF9):c.101-42_101-3del
NM_001561.6(TNFRSF9):c.101-6_101-3del rs555590077
NM_001561.6(TNFRSF9):c.115A>G (p.Asn39Asp) rs1173865364
NM_001561.6(TNFRSF9):c.140C>T (p.Pro47Leu)
NM_001561.6(TNFRSF9):c.163del (p.Ser55fs)
NM_001561.6(TNFRSF9):c.165C>A (p.Ser55Arg) rs150479025
NM_001561.6(TNFRSF9):c.183C>T (p.Thr61=)
NM_001561.6(TNFRSF9):c.195C>T (p.Cys65=)
NM_001561.6(TNFRSF9):c.197G>A (p.Arg66Lys)
NM_001561.6(TNFRSF9):c.205A>G (p.Lys69Glu) rs2151420195
NM_001561.6(TNFRSF9):c.208+10C>T
NM_001561.6(TNFRSF9):c.208+11A>G
NM_001561.6(TNFRSF9):c.208+15A>G
NM_001561.6(TNFRSF9):c.208+17A>G
NM_001561.6(TNFRSF9):c.208+5_208+16del rs375937837
NM_001561.6(TNFRSF9):c.209-10G>T
NM_001561.6(TNFRSF9):c.209-18G>T
NM_001561.6(TNFRSF9):c.209-4G>A
NM_001561.6(TNFRSF9):c.215T>C (p.Phe72Ser) rs2151420079
NM_001561.6(TNFRSF9):c.245G>A (p.Ser82Asn)
NM_001561.6(TNFRSF9):c.266C>T (p.Thr89Ile)
NM_001561.6(TNFRSF9):c.273G>A (p.Gly91=)
NM_001561.6(TNFRSF9):c.283C>T (p.Leu95=)
NM_001561.6(TNFRSF9):c.302del (p.Met101fs)
NM_001561.6(TNFRSF9):c.310C>T (p.Gln104Ter)
NM_001561.6(TNFRSF9):c.322C>G (p.Gln108Glu) rs147680622
NM_001561.6(TNFRSF9):c.328_332del (p.Gln110fs)
NM_001561.6(TNFRSF9):c.345dup (p.Gly116fs)
NM_001561.6(TNFRSF9):c.346+4C>G rs9657966
NM_001561.6(TNFRSF9):c.346+4C>T
NM_001561.6(TNFRSF9):c.346+5G>A
NM_001561.6(TNFRSF9):c.347-13T>A
NM_001561.6(TNFRSF9):c.347-15C>A
NM_001561.6(TNFRSF9):c.347-18T>C
NM_001561.6(TNFRSF9):c.347-20G>T
NM_001561.6(TNFRSF9):c.347-3A>G
NM_001561.6(TNFRSF9):c.347-9T>A
NM_001561.6(TNFRSF9):c.347G>C (p.Gly116Ala)
NM_001561.6(TNFRSF9):c.355G>C (p.Asp119His)
NM_001561.6(TNFRSF9):c.357C>G (p.Asp119Glu)
NM_001561.6(TNFRSF9):c.36G>C (p.Leu12=)
NM_001561.6(TNFRSF9):c.381T>C (p.Asp127=)
NM_001561.6(TNFRSF9):c.388C>T (p.Arg130Cys)
NM_001561.6(TNFRSF9):c.389G>A (p.Arg130His)
NM_001561.6(TNFRSF9):c.391_392delinsAT (p.Gly131Ile)
NM_001561.6(TNFRSF9):c.405C>T (p.Pro135=)
NM_001561.6(TNFRSF9):c.413+20G>T
NM_001561.6(TNFRSF9):c.413+2T>C
NM_001561.6(TNFRSF9):c.414-4T>C
NM_001561.6(TNFRSF9):c.421T>C (p.Leu141=)
NM_001561.6(TNFRSF9):c.425A>T (p.Asp142Val) rs1578076558
NM_001561.6(TNFRSF9):c.428G>C (p.Gly143Ala)
NM_001561.6(TNFRSF9):c.428G>T (p.Gly143Val)
NM_001561.6(TNFRSF9):c.433T>G (p.Ser145Ala) rs1220227331
NM_001561.6(TNFRSF9):c.439C>T (p.Leu147Phe)
NM_001561.6(TNFRSF9):c.450G>A (p.Gly150=)
NM_001561.6(TNFRSF9):c.453G>A (p.Thr151=)
NM_001561.6(TNFRSF9):c.454A>G (p.Lys152Glu)
NM_001561.6(TNFRSF9):c.45C>T (p.Val15=)
NM_001561.6(TNFRSF9):c.478C>T (p.Pro160Ser)
NM_001561.6(TNFRSF9):c.489C>T (p.Ala163=)
NM_001561.6(TNFRSF9):c.510C>T (p.Ser170=)
NM_001561.6(TNFRSF9):c.521C>T (p.Pro174Leu)
NM_001561.6(TNFRSF9):c.522G>A (p.Pro174=)
NM_001561.6(TNFRSF9):c.534G>A (p.Ala178=)
NM_001561.6(TNFRSF9):c.544+13T>C
NM_001561.6(TNFRSF9):c.544+16C>T
NM_001561.6(TNFRSF9):c.544+3A>G
NM_001561.6(TNFRSF9):c.544+7G>T rs1434417143
NM_001561.6(TNFRSF9):c.544+8G>T
NM_001561.6(TNFRSF9):c.544+8_544+12dup
NM_001561.6(TNFRSF9):c.545-11G>A
NM_001561.6(TNFRSF9):c.545-13C>G
NM_001561.6(TNFRSF9):c.545-1G>A rs2151417795
NM_001561.6(TNFRSF9):c.555G>A (p.Pro185=) rs150424591
NM_001561.6(TNFRSF9):c.555G>T (p.Pro185=)
NM_001561.6(TNFRSF9):c.558G>A (p.Gln186=)
NM_001561.6(TNFRSF9):c.561C>A (p.Ile187=)
NM_001561.6(TNFRSF9):c.567CTT[1] (p.Phe191del) rs753979152
NM_001561.6(TNFRSF9):c.573del (p.Ala193fs) rs1639761448
NM_001561.6(TNFRSF9):c.579G>A (p.Ala193=) rs192265662
NM_001561.6(TNFRSF9):c.579G>T (p.Ala193=)
NM_001561.6(TNFRSF9):c.594G>A (p.Ala198=)
NM_001561.6(TNFRSF9):c.601T>C (p.Phe201Leu)
NM_001561.6(TNFRSF9):c.605T>C (p.Leu202Pro) rs770098625
NM_001561.6(TNFRSF9):c.609G>A (p.Leu203=)
NM_001561.6(TNFRSF9):c.615C>T (p.Phe205=)
NM_001561.6(TNFRSF9):c.620C>T (p.Thr207Met)
NM_001561.6(TNFRSF9):c.621G>T (p.Thr207=)
NM_001561.6(TNFRSF9):c.663G>A (p.Leu221=)
NM_001561.6(TNFRSF9):c.665A>G (p.Tyr222Cys)
NM_001561.6(TNFRSF9):c.668T>C (p.Ile223Thr)
NM_001561.6(TNFRSF9):c.679+13T>C
NM_001561.6(TNFRSF9):c.679+15A>G
NM_001561.6(TNFRSF9):c.679+1G>A
NM_001561.6(TNFRSF9):c.680-12dup rs767796238
NM_001561.6(TNFRSF9):c.680-15A>T
NM_001561.6(TNFRSF9):c.680-3del rs767796238
NM_001561.6(TNFRSF9):c.680-7T>G rs1361632057
NM_001561.6(TNFRSF9):c.680-8T>G
NM_001561.6(TNFRSF9):c.684T>C (p.Phe228=)
NM_001561.6(TNFRSF9):c.693A>G (p.Pro231=) rs750218461
NM_001561.6(TNFRSF9):c.695T>C (p.Val232Ala)
NM_001561.6(TNFRSF9):c.6A>G (p.Gly2=)
NM_001561.6(TNFRSF9):c.708A>C (p.Gln236His)
NM_001561.6(TNFRSF9):c.730C>T (p.Arg244Ter) rs1280784319
NM_001561.6(TNFRSF9):c.731G>A (p.Arg244Gln)
NM_001561.6(TNFRSF9):c.740A>G (p.Glu247Gly)
NM_001561.6(TNFRSF9):c.740AAG[3] (p.Glu250del)
NM_001561.6(TNFRSF9):c.748_749insGAG (p.Glu249_Glu250insGly)
NM_001561.6(TNFRSF9):c.763C>T (p.Leu255=) rs2151410080
NM_001561.6(TNFRSF9):c.78T>C (p.Asp26=)

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