ClinVar Miner

List of variants in gene FBXO7 studied for Parkinson disease

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_001033024.1(FBXO7):c.35T>G (p.Leu12Arg) rs8137714
NM_012179.3(FBXO7):c.1132C>G (p.Arg378Gly) rs71799110
NM_012179.3(FBXO7):c.1144+1G>T rs730880272
NM_012179.3(FBXO7):c.1144+9C>T rs199954341
NM_012179.3(FBXO7):c.122+9G>A rs192327462
NM_012179.3(FBXO7):c.1492C>T (p.Arg498Ter) rs121918304
NM_012179.3(FBXO7):c.151delA (p.Asn51Thrfs) rs1228608709
NM_012179.3(FBXO7):c.1546G>C (p.Asp516His) rs34316445
NM_012179.3(FBXO7):c.260T>C (p.Ile87Thr) rs780055842
NM_012179.3(FBXO7):c.345G>A (p.Met115Ile) rs11107
NM_012179.3(FBXO7):c.540A>G (p.Pro180=) rs41311141
NM_012179.3(FBXO7):c.601G>A (p.Val201Met) rs61730783
NM_012179.3(FBXO7):c.65C>T (p.Thr22Met) rs121918305
NM_012179.3(FBXO7):c.693C>T (p.Ser231=) rs61752254
NM_012179.3(FBXO7):c.949C>T (p.Leu317=) rs9726
NM_012179.3(FBXO7):c.[274G>C];[520T>A]
NM_012179.4(FBXO7):c.1263_1267CATTC[3] (p.Tyr425Hisfs)
NM_012179.4(FBXO7):c.722_723CT[2] (p.Cys243Argfs)

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