ClinVar Miner

List of variants in gene TGFBR2 studied for not provided

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Total variants: 120
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HGVS dbSNP
GRCh37/hg19 3p24.1(chr3:30684776-30698392)x1
NM_003242.6(TGFBR2):c.-128C>G rs2306856
NM_003242.6(TGFBR2):c.-27G>C rs1469986980
NM_003242.6(TGFBR2):c.1016G>T (p.Arg339Leu) rs727503473
NM_003242.6(TGFBR2):c.1029C>T (p.Ser343=) rs1060504407
NM_003242.6(TGFBR2):c.1043G>A (p.Arg348His) rs369450067
NM_003242.6(TGFBR2):c.1063G>A (p.Ala355Thr) rs104893813
NM_003242.6(TGFBR2):c.1066C>G (p.Arg356Gly) rs199660234
NM_003242.6(TGFBR2):c.1066C>T (p.Arg356Trp) rs199660234
NM_003242.6(TGFBR2):c.106A>G (p.Met36Val) rs17025864
NM_003242.6(TGFBR2):c.1071G>A (p.Gly357=) rs1575158015
NM_003242.6(TGFBR2):c.1078C>G (p.His360Asp) rs189119533
NM_003242.6(TGFBR2):c.1085A>G (p.His362Arg) rs863223842
NM_003242.6(TGFBR2):c.1116G>A (p.Lys372=) rs753782498
NM_003242.6(TGFBR2):c.1119G>A (p.Met373Ile) rs35719192
NM_003242.6(TGFBR2):c.1120C>T (p.Pro374Ser) rs863223843
NM_003242.6(TGFBR2):c.1121C>T (p.Pro374Leu) rs1057524399
NM_003242.6(TGFBR2):c.1134G>T (p.Arg378Ser) rs1575158079
NM_003242.6(TGFBR2):c.1145G>A (p.Ser382Asn) rs863223844
NM_003242.6(TGFBR2):c.1156C>T (p.Leu386Phe) rs1575158103
NM_003242.6(TGFBR2):c.115A>T (p.Thr39Ser) rs780280433
NM_003242.6(TGFBR2):c.1171C>T (p.Leu391=) rs779762218
NM_003242.6(TGFBR2):c.1190A>G (p.Asp397Gly) rs863223846
NM_003242.6(TGFBR2):c.1215C>G (p.Asp405Glu) rs1575158153
NM_003242.6(TGFBR2):c.1217C>T (p.Pro406Leu) rs748480163
NM_003242.6(TGFBR2):c.1241C>T (p.Ala414Val)
NM_003242.6(TGFBR2):c.1254+8A>G rs200630803
NM_003242.6(TGFBR2):c.1255-7G>T rs1575158857
NM_003242.6(TGFBR2):c.1255G>T (p.Val419Leu) rs863223847
NM_003242.6(TGFBR2):c.1256T>A (p.Val419Glu) rs863223848
NM_003242.6(TGFBR2):c.1267_1269dup (p.Arg423dup) rs1575158901
NM_003242.6(TGFBR2):c.126C>T (p.Asn42=) rs574133875
NM_003242.6(TGFBR2):c.1270T>C (p.Tyr424His) rs1559467821
NM_003242.6(TGFBR2):c.1276G>A (p.Ala426Thr) rs863223849
NM_003242.6(TGFBR2):c.1277C>A (p.Ala426Asp) rs730880224
NM_003242.6(TGFBR2):c.1279C>T (p.Pro427Ser) rs863223850
NM_003242.6(TGFBR2):c.1314T>C (p.Asn438=) rs772490613
NM_003242.6(TGFBR2):c.1336G>A (p.Asp446Asn) rs886039551
NM_003242.6(TGFBR2):c.1338T>G (p.Asp446Glu) rs863223851
NM_003242.6(TGFBR2):c.135C>T (p.Val45=) rs1575143681
NM_003242.6(TGFBR2):c.136A>T (p.Lys46Ter) rs1553627148
NM_003242.6(TGFBR2):c.1378C>T (p.Arg460Cys) rs104893811
NM_003242.6(TGFBR2):c.1379G>A (p.Arg460His) rs104893816
NM_003242.6(TGFBR2):c.1397-116G>A rs11466526
NM_003242.6(TGFBR2):c.1397-140A>C rs11466525
NM_003242.6(TGFBR2):c.1397-240G>A rs9843942
NM_003242.6(TGFBR2):c.1410T>G (p.Tyr470Ter) rs1553631696
NM_003242.6(TGFBR2):c.1418C>T (p.Pro473Leu) rs397516839
NM_003242.6(TGFBR2):c.1471G>A (p.Val491Met) rs754176932
NM_003242.6(TGFBR2):c.1483C>T (p.Arg495Ter) rs104893819
NM_003242.6(TGFBR2):c.1489C>T (p.Arg497Ter) rs863223852
NM_003242.6(TGFBR2):c.1492C>T (p.Pro498Ser)
NM_003242.6(TGFBR2):c.1521C>T (p.His507=) rs544130308
NM_003242.6(TGFBR2):c.1524+10G>C rs377397188
NM_003242.6(TGFBR2):c.1524+230C>G rs9819937
NM_003242.6(TGFBR2):c.1525-5T>C rs770896804
NM_003242.6(TGFBR2):c.1525-7G>A rs377499122
NM_003242.6(TGFBR2):c.1526G>T (p.Gly509Val) rs863223853
NM_003242.6(TGFBR2):c.1542T>C (p.Cys514=) rs1575166645
NM_003242.6(TGFBR2):c.1546A>T (p.Thr516Ser) rs370708687
NM_003242.6(TGFBR2):c.1548G>A (p.Thr516=) rs140662877
NM_003242.6(TGFBR2):c.1564G>A (p.Asp522Asn) rs863223854
NM_003242.6(TGFBR2):c.1570G>A (p.Asp524Asn) rs727504421
NM_003242.6(TGFBR2):c.1582C>T (p.Arg528Cys) rs104893810
NM_003242.6(TGFBR2):c.1583G>A (p.Arg528His) rs104893815
NM_003242.6(TGFBR2):c.1587C>T (p.Leu529=) rs761435905
NM_003242.6(TGFBR2):c.1609C>T (p.Arg537Cys) rs104893809
NM_003242.6(TGFBR2):c.1610G>A (p.Arg537His) rs1057524810
NM_003242.6(TGFBR2):c.1645G>T (p.Gly549Trp) rs748418894
NM_003242.6(TGFBR2):c.1657T>A (p.Ser553Thr) rs112215250
NM_003242.6(TGFBR2):c.1668G>A (p.Lys556=) rs779923854
NM_003242.6(TGFBR2):c.222C>T (p.Thr74=) rs112864356
NM_003242.6(TGFBR2):c.264-289G>A rs6790706
NM_003242.6(TGFBR2):c.264-35T>G rs11466495
NM_003242.6(TGFBR2):c.276C>T (p.Asp92=) rs774840447
NM_003242.6(TGFBR2):c.296C>T (p.Thr99Ile) rs863223837
NM_003242.6(TGFBR2):c.297A>G (p.Thr99=) rs727504343
NM_003242.6(TGFBR2):c.326A>T (p.His109Leu) rs1553627759
NM_003242.6(TGFBR2):c.33G>T (p.Pro11=) rs1575125895
NM_003242.6(TGFBR2):c.367A>T (p.Met123Leu) rs768385200
NM_003242.6(TGFBR2):c.412T>G (p.Cys138Gly) rs863223838
NM_003242.6(TGFBR2):c.454+267T>C rs2029314
NM_003242.6(TGFBR2):c.454+74A>G rs11466496
NM_003242.6(TGFBR2):c.454G>A (p.Glu152Lys) rs778675253
NM_003242.6(TGFBR2):c.455-2del rs863223855
NM_003242.6(TGFBR2):c.455-303A>C rs11466511
NM_003242.6(TGFBR2):c.533T>A (p.Val178Asp) rs1553630079
NM_003242.6(TGFBR2):c.551T>A (p.Ile184Asn) rs863223839
NM_003242.6(TGFBR2):c.556T>A (p.Phe186Ile) rs368346624
NM_003242.6(TGFBR2):c.571G>A (p.Val191Ile) rs56105708
NM_003242.6(TGFBR2):c.617C>T (p.Thr206Met) rs150022335
NM_003242.6(TGFBR2):c.620G>A (p.Arg207Gln) rs371209879
NM_003242.6(TGFBR2):c.621G>A (p.Arg207=) rs886058304
NM_003242.6(TGFBR2):c.649G>C (p.Ala217Pro) rs149141477
NM_003242.6(TGFBR2):c.666T>C (p.Asp222=) rs755404252
NM_003242.6(TGFBR2):c.690G>A (p.Thr230=) rs201560560
NM_003242.6(TGFBR2):c.6T>C (p.Gly2=) rs758864131
NM_003242.6(TGFBR2):c.701A>T (p.Asn234Ile) rs863223840
NM_003242.6(TGFBR2):c.757G>A (p.Gly253Ser) rs1559466824
NM_003242.6(TGFBR2):c.75A>G (p.Pro25=) rs572435149
NM_003242.6(TGFBR2):c.760C>T (p.Arg254Cys) rs863223856
NM_003242.6(TGFBR2):c.845_853del (p.Glu282_Tyr284del) rs1085307498
NM_003242.6(TGFBR2):c.902A>G (p.His301Arg) rs863223857
NM_003242.6(TGFBR2):c.907A>C (p.Asn303His) rs773932892
NM_003242.6(TGFBR2):c.913C>T (p.Leu305Phe) rs1553630171
NM_003242.6(TGFBR2):c.927G>A (p.Thr309=) rs756625146
NM_003242.6(TGFBR2):c.930T>C (p.Ala310=) rs1341666511
NM_003242.6(TGFBR2):c.938G>A (p.Arg313Gln) rs200361387
NM_003242.6(TGFBR2):c.94+16236G>A rs1409106424
NM_003242.6(TGFBR2):c.94+16256C>T rs143701368
NM_003242.6(TGFBR2):c.94+16260C>G rs113474008
NM_003242.6(TGFBR2):c.94+16273G>A rs781529108
NM_003242.6(TGFBR2):c.94+16278G>C rs557449314
NM_003242.6(TGFBR2):c.94+16293C>A rs138262219
NM_003242.6(TGFBR2):c.95-3C>A rs375330013
NM_003242.6(TGFBR2):c.964T>G (p.Trp322Gly) rs863223858
NM_003242.6(TGFBR2):c.975C>T (p.Thr325=) rs532098604
NM_003242.6(TGFBR2):c.984C>T (p.His328=) rs193922666
NM_003242.6(TGFBR2):c.998T>A (p.Leu333Gln) rs863223841
NM_003242.6(TGFBR2):c.999A>G (p.Leu333=) rs2229102

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