ClinVar Miner

List of variants in gene FBXO7 studied for Parkinson disease

Included ClinVar conditions (34):
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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP
NM_012179.3(FBXO7):c.[274G>C];[520T>A]
NM_012179.4(FBXO7):c.*104T>C
NM_012179.4(FBXO7):c.*170C>G rs186797068
NM_012179.4(FBXO7):c.*198T>G
NM_012179.4(FBXO7):c.*263A>G rs886057422
NM_012179.4(FBXO7):c.*282A>T rs886057423
NM_012179.4(FBXO7):c.*47A>T rs367714958
NM_012179.4(FBXO7):c.*82G>A
NM_012179.4(FBXO7):c.-118T>G rs886057418
NM_012179.4(FBXO7):c.-130C>T
NM_012179.4(FBXO7):c.-168A>G rs886057417
NM_012179.4(FBXO7):c.-184C>T rs11538371
NM_012179.4(FBXO7):c.-93G>A rs886057419
NM_012179.4(FBXO7):c.-97C>T
NM_012179.4(FBXO7):c.1054G>A (p.Val352Ile) rs762037477
NM_012179.4(FBXO7):c.1070C>T (p.Ala357Val) rs141068487
NM_012179.4(FBXO7):c.1125A>G (p.Leu375=) rs147911892
NM_012179.4(FBXO7):c.1132C>G (p.Arg378Gly) rs71799110
NM_012179.4(FBXO7):c.1144+1G>T rs730880272
NM_012179.4(FBXO7):c.1144+9C>T rs199954341
NM_012179.4(FBXO7):c.1181_1182+1del
NM_012179.4(FBXO7):c.1198C>A (p.His400Asn)
NM_012179.4(FBXO7):c.1206_1207dup (p.Arg403fs) rs749019340
NM_012179.4(FBXO7):c.122+272T>G rs8137714
NM_012179.4(FBXO7):c.122+9G>A rs192327462
NM_012179.4(FBXO7):c.1263_1267CATTC[3] (p.Tyr425fs) rs749534144
NM_012179.4(FBXO7):c.1264A>T (p.Ile422Phe)
NM_012179.4(FBXO7):c.1266T>G (p.Ile422Met)
NM_012179.4(FBXO7):c.1271_1272delinsAT (p.Phe424Tyr) rs1601520476
NM_012179.4(FBXO7):c.1332C>G (p.Ile444Met)
NM_012179.4(FBXO7):c.1385G>T (p.Ser462Ile) rs149552421
NM_012179.4(FBXO7):c.1441C>T (p.Arg481Cys) rs148272407
NM_012179.4(FBXO7):c.1453G>A (p.Val485Ile) rs141286570
NM_012179.4(FBXO7):c.1492C>T (p.Arg498Ter) rs121918304
NM_012179.4(FBXO7):c.1497C>T (p.Gly499=)
NM_012179.4(FBXO7):c.1505A>G (p.Asn502Ser) rs144538200
NM_012179.4(FBXO7):c.1506T>C (p.Asn502=)
NM_012179.4(FBXO7):c.1527C>A (p.Pro509=) rs758609287
NM_012179.4(FBXO7):c.152del (p.Asn51fs) rs1228608709
NM_012179.4(FBXO7):c.1535G>A (p.Gly512Asp) rs142471722
NM_012179.4(FBXO7):c.1536_1539del (p.Arg513fs) rs772175765
NM_012179.4(FBXO7):c.1546G>C (p.Asp516His) rs34316445
NM_012179.4(FBXO7):c.1552C>T (p.Arg518Trp)
NM_012179.4(FBXO7):c.155A>G (p.Tyr52Cys)
NM_012179.4(FBXO7):c.169A>G (p.Thr57Ala) rs760306475
NM_012179.4(FBXO7):c.260T>C (p.Ile87Thr) rs780055842
NM_012179.4(FBXO7):c.274G>C (p.Asp92His) rs139135860
NM_012179.4(FBXO7):c.277T>G (p.Ser93Ala)
NM_012179.4(FBXO7):c.32C>T (p.Thr11Ile)
NM_012179.4(FBXO7):c.345G>A (p.Met115Ile) rs11107
NM_012179.4(FBXO7):c.358C>T (p.Pro120Ser) rs191469599
NM_012179.4(FBXO7):c.367T>G (p.Ser123Ala)
NM_012179.4(FBXO7):c.447G>A (p.Glu149=)
NM_012179.4(FBXO7):c.464C>A (p.Ala155Glu)
NM_012179.4(FBXO7):c.49C>G (p.Pro17Ala) rs886057420
NM_012179.4(FBXO7):c.540A>G (p.Pro180=) rs41311141
NM_012179.4(FBXO7):c.593C>G (p.Ala198Gly)
NM_012179.4(FBXO7):c.601G>A (p.Val201Met) rs61730783
NM_012179.4(FBXO7):c.65C>T (p.Thr22Met) rs121918305
NM_012179.4(FBXO7):c.693C>T (p.Ser231=) rs61752254
NM_012179.4(FBXO7):c.697G>A (p.Val233Met) rs1388222868
NM_012179.4(FBXO7):c.722_723CT[2] (p.Cys243fs) rs1290655316
NM_012179.4(FBXO7):c.745A>G (p.Thr249Ala) rs749742547
NM_012179.4(FBXO7):c.949C>T (p.Leu317=) rs9726
NM_012179.4(FBXO7):c.957T>C (p.Phe319=)
NM_012179.4(FBXO7):c.968-14T>G

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