ClinVar Miner

List of variants in gene FBXO11 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001190274.2(FBXO11):c.1065ACA[1] (p.Gln356del)
NM_001190274.2(FBXO11):c.1070A>C (p.His357Pro) rs998477796
NM_001190274.2(FBXO11):c.1118T>A (p.Ile373Asn) rs766012117
NM_001190274.2(FBXO11):c.1148G>A (p.Cys383Tyr)
NM_001190274.2(FBXO11):c.1200C>G (p.Ile400Met)
NM_001190274.2(FBXO11):c.1208G>A (p.Cys403Tyr)
NM_001190274.2(FBXO11):c.1223G>T (p.Cys408Phe)
NM_001190274.2(FBXO11):c.1228A>G (p.Asn410Asp)
NM_001190274.2(FBXO11):c.1286C>A (p.Ser429Tyr) rs773388275
NM_001190274.2(FBXO11):c.1346A>T (p.Asn449Ile)
NM_001190274.2(FBXO11):c.1363C>T (p.Arg455Cys)
NM_001190274.2(FBXO11):c.1364G>A (p.Arg455His) rs2104807681
NM_001190274.2(FBXO11):c.1395C>T (p.Gly465=)
NM_001190274.2(FBXO11):c.1398+13_1398+16del rs67864921
NM_001190274.2(FBXO11):c.1400G>A (p.Gly467Asp) rs2104739734
NM_001190274.2(FBXO11):c.1424A>G (p.His475Arg)
NM_001190274.2(FBXO11):c.147_182dup (p.Gln50_Pro61dup) rs1478658114
NM_001190274.2(FBXO11):c.1501C>T (p.Gln501Ter) rs1558414256
NM_001190274.2(FBXO11):c.1510G>A (p.Gly504Arg)
NM_001190274.2(FBXO11):c.1515A>G (p.Ile505Met)
NM_001190274.2(FBXO11):c.1526A>C (p.Glu509Ala)
NM_001190274.2(FBXO11):c.1537G>A (p.Gly513Arg) rs2104738949
NM_001190274.2(FBXO11):c.1582G>A (p.Val528Ile)
NM_001190274.2(FBXO11):c.1601G>C (p.Ser534Thr)
NM_001190274.2(FBXO11):c.1646G>A (p.Gly549Glu)
NM_001190274.2(FBXO11):c.1696A>G (p.Ile566Val)
NM_001190274.2(FBXO11):c.1714G>A (p.Ala572Thr)
NM_001190274.2(FBXO11):c.171_173dup (p.Pro66_Leu67insPro)
NM_001190274.2(FBXO11):c.1760A>T (p.Asn587Ile)
NM_001190274.2(FBXO11):c.1797G>A (p.Val599=)
NM_001190274.2(FBXO11):c.1997T>G (p.Val666Gly) rs2104701993
NM_001190274.2(FBXO11):c.2041A>G (p.Ile681Val)
NM_001190274.2(FBXO11):c.2120A>G (p.Asn707Ser) rs1670752914
NM_001190274.2(FBXO11):c.2159C>T (p.Pro720Leu)
NM_001190274.2(FBXO11):c.2168GAA[1] (p.Arg724del)
NM_001190274.2(FBXO11):c.2207G>T (p.Cys736Phe)
NM_001190274.2(FBXO11):c.2278A>G (p.Ile760Val)
NM_001190274.2(FBXO11):c.2321T>C (p.Phe774Ser) rs2104633091
NM_001190274.2(FBXO11):c.2335G>A (p.Ala779Thr)
NM_001190274.2(FBXO11):c.407G>T (p.Arg136Leu)
NM_001190274.2(FBXO11):c.427T>G (p.Ser143Ala) rs1284695050
NM_001190274.2(FBXO11):c.458A>G (p.Gln153Arg)
NM_001190274.2(FBXO11):c.500TCT[1] (p.Phe168del) rs2104856413
NM_001190274.2(FBXO11):c.539C>G (p.Ala180Gly)
NM_001190274.2(FBXO11):c.544G>A (p.Val182Ile) rs2104856155
NM_001190274.2(FBXO11):c.601A>G (p.Met201Val)
NM_001190274.2(FBXO11):c.643C>T (p.Pro215Ser) rs1387053758
NM_001190274.2(FBXO11):c.682C>T (p.His228Tyr)
NM_001190274.2(FBXO11):c.683A>C (p.His228Pro) rs1398888171
NM_001190274.2(FBXO11):c.700G>C (p.Glu234Gln)
NM_001190274.2(FBXO11):c.703A>G (p.Ser235Gly)
NM_001190274.2(FBXO11):c.710A>G (p.Gln237Arg) rs2104831924
NM_001190274.2(FBXO11):c.733G>T (p.Val245Leu)
NM_001190274.2(FBXO11):c.884A>G (p.Tyr295Cys)
NM_001190274.2(FBXO11):c.905T>C (p.Ile302Thr) rs1553341071
NM_001190274.2(FBXO11):c.914C>A (p.Pro305Gln) rs2104823139
NM_001190274.2(FBXO11):c.945A>C (p.Lys315Asn) rs139178411
NM_001190274.2(FBXO11):c.962T>C (p.Ile321Thr)
NM_001190274.2(FBXO11):c.964A>G (p.Ile322Val)
NM_001190274.2(FBXO11):c.965T>C (p.Ile322Thr)
NM_001190274.2(FBXO11):c.967G>C (p.Glu323Gln)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.