ClinVar Miner

List of variants in gene AGXT reported as uncertain significance

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Gene type:
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Total variants: 84
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HGVS dbSNP
NM_000030.2:c.165+15_166-18dup
NM_000030.3(AGXT):c.*160G>A rs776483024
NM_000030.3(AGXT):c.*162A>G rs886055844
NM_000030.3(AGXT):c.*19G>A rs143458283
NM_000030.3(AGXT):c.*289A>C rs4344931
NM_000030.3(AGXT):c.*39G>A rs369979466
NM_000030.3(AGXT):c.*41C>A rs4273214
NM_000030.3(AGXT):c.-14G>A rs376396832
NM_000030.3(AGXT):c.1020A>G (p.Ile340Met) rs4426527
NM_000030.3(AGXT):c.1071+12C>T rs375775541
NM_000030.3(AGXT):c.1071+13G>A rs758413374
NM_000030.3(AGXT):c.1072-91G>A rs180177159
NM_000030.3(AGXT):c.1111G>A (p.Glu371Lys) rs369664123
NM_000030.3(AGXT):c.1142G>A (p.Arg381Lys) rs151185188
NM_000030.3(AGXT):c.1174C>T (p.Leu392=) rs180177167
NM_000030.3(AGXT):c.145A>C (p.Met49Leu) rs74205173
NM_000030.3(AGXT):c.165+12G>C rs201989825
NM_000030.3(AGXT):c.165+16A>G rs66494441
NM_000030.3(AGXT):c.165+19_166-48dup rs180177174
NM_000030.3(AGXT):c.165+40A>C rs57017537
NM_000030.3(AGXT):c.165+44T>A rs58120546
NM_000030.3(AGXT):c.166-14C>T rs180177176
NM_000030.3(AGXT):c.166-47T>C rs180177178
NM_000030.3(AGXT):c.166-54C>T rs180177179
NM_000030.3(AGXT):c.166-56C>T rs114401766
NM_000030.3(AGXT):c.166-57C>T rs180177175
NM_000030.3(AGXT):c.260_271del (p.Glu87_Leu90del) rs1553648333
NM_000030.3(AGXT):c.264C>T (p.Ala88=) rs35698882
NM_000030.3(AGXT):c.26C>A (p.Thr9Asn) rs115014558
NM_000030.3(AGXT):c.27C>A (p.Thr9=) rs180177188
NM_000030.3(AGXT):c.28C>G (p.Pro10Ala) rs180177191
NM_000030.3(AGXT):c.296C>A (p.Ser99Tyr) rs180177192
NM_000030.3(AGXT):c.32C>A (p.Pro11His) rs34116584
NM_000030.3(AGXT):c.32C>T (p.Pro11Leu) rs34116584
NM_000030.3(AGXT):c.352C>T (p.Arg118Cys) rs376844297
NM_000030.3(AGXT):c.358+13C>T rs34995778
NM_000030.3(AGXT):c.358+56_358+64del rs180177209
NM_000030.3(AGXT):c.35A>G (p.Lys12Arg) rs142969817
NM_000030.3(AGXT):c.385G>C (p.Asp129His) rs180177212
NM_000030.3(AGXT):c.423+29C>T rs117043148
NM_000030.3(AGXT):c.423+36A>C rs180177216
NM_000030.3(AGXT):c.423+45T>G rs117357855
NM_000030.3(AGXT):c.423G>C (p.Glu141Asp) rs180177217
NM_000030.3(AGXT):c.424-12dup rs398122323
NM_000030.3(AGXT):c.424-16G>A rs74895925
NM_000030.3(AGXT):c.484G>A (p.Val162Met) rs147497484
NM_000030.3(AGXT):c.489G>A (p.Leu163=) rs147601535
NM_000030.3(AGXT):c.524+3G>A rs886055839
NM_000030.3(AGXT):c.524+6C>A rs770992934
NM_000030.3(AGXT):c.524+91C>T rs10196315
NM_000030.3(AGXT):c.557C>T (p.Ala186Val) rs117195882
NM_000030.3(AGXT):c.590G>A (p.Arg197Gln) rs34664134
NM_000030.3(AGXT):c.601G>A (p.Asp201Asn) rs886055840
NM_000030.3(AGXT):c.654G>A (p.Ser218=) rs33958047
NM_000030.3(AGXT):c.65A>G (p.Asn22Ser) rs34885252
NM_000030.3(AGXT):c.676G>A (p.Ala226Thr) rs749577985
NM_000030.3(AGXT):c.680+130C>T rs78178548
NM_000030.3(AGXT):c.680+17C>T rs11693280
NM_000030.3(AGXT):c.680+75G>A rs117619103
NM_000030.3(AGXT):c.681-94G>A rs141154272
NM_000030.3(AGXT):c.683_685AGA[3] (p.Lys229dup) rs1553648979
NM_000030.3(AGXT):c.705G>A (p.Thr235=) rs35977912
NM_000030.3(AGXT):c.742G>T (p.Ala248Ser) rs180177260
NM_000030.3(AGXT):c.743C>T (p.Ala248Val) rs372482918
NM_000030.3(AGXT):c.777-44A>G rs12464426
NM_000030.3(AGXT):c.777-45C>T rs12478859
NM_000030.3(AGXT):c.781C>G (p.His261Asp) rs778567956
NM_000030.3(AGXT):c.822G>C (p.Glu274Asp) rs146525143
NM_000030.3(AGXT):c.82C>T (p.Pro28Ser) rs376684240
NM_000030.3(AGXT):c.836T>C (p.Ile279Thr) rs140992177
NM_000030.3(AGXT):c.837T>G (p.Ile279Met) rs180177277
NM_000030.3(AGXT):c.839C>T (p.Ala280Val) rs73106685
NM_000030.3(AGXT):c.845A>G (p.Gln282Arg) rs180177280
NM_000030.3(AGXT):c.846+52G>A rs12695032
NM_000030.3(AGXT):c.865C>T (p.Arg289Cys) rs180177290
NM_000030.3(AGXT):c.866G>A (p.Arg289His) rs61729604
NM_000030.3(AGXT):c.883G>A (p.Ala295Thr) rs13408961
NM_000030.3(AGXT):c.901C>T (p.Arg301Cys) rs886055841
NM_000030.3(AGXT):c.930C>T (p.Phe310=) rs886055842
NM_000030.3(AGXT):c.942+14T>G rs886055843
NM_000030.3(AGXT):c.943-117C>T rs10199038
NM_000030.3(AGXT):c.949C>T (p.Arg317Trp) rs774030578
NM_000030.3(AGXT):c.976G>A (p.Val326Ile) rs115057148
Single allele

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