ClinVar Miner

List of variants in gene FBXO39 reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_153230.3(FBXO39):c.881A>G (p.Lys294Arg) rs142087585 0.00030
NM_153230.3(FBXO39):c.866T>C (p.Phe289Ser) rs200774821 0.00023
NM_153230.3(FBXO39):c.871C>T (p.Arg291Trp) rs149057361 0.00023
NM_153230.3(FBXO39):c.983C>T (p.Thr328Ile) rs200108762 0.00013
NM_153230.3(FBXO39):c.170G>A (p.Arg57Gln) rs140674090 0.00011
NM_153230.3(FBXO39):c.31C>G (p.Gln11Glu) rs770428705 0.00009
NM_153230.3(FBXO39):c.889C>T (p.Arg297Cys) rs747537634 0.00006
NM_153230.3(FBXO39):c.337C>T (p.Arg113Trp) rs373411596 0.00005
NM_153230.3(FBXO39):c.477G>T (p.Lys159Asn) rs375015434 0.00005
NM_153230.3(FBXO39):c.338G>A (p.Arg113Gln) rs763737793 0.00003
NM_153230.3(FBXO39):c.755G>A (p.Arg252Gln) rs200692290 0.00003
NM_153230.3(FBXO39):c.1219A>G (p.Arg407Gly) rs775749801 0.00002
NM_153230.3(FBXO39):c.473A>G (p.Lys158Arg) rs1009302010 0.00002
NM_153230.3(FBXO39):c.769A>C (p.Lys257Gln) rs750415033 0.00002
NM_153230.3(FBXO39):c.845A>G (p.Asn282Ser) rs750586807 0.00002
NM_153230.3(FBXO39):c.1034G>A (p.Cys345Tyr) rs762799823 0.00001
NM_153230.3(FBXO39):c.1069G>C (p.Glu357Gln) rs1225965291 0.00001
NM_153230.3(FBXO39):c.283A>C (p.Lys95Gln) rs747260135 0.00001
NM_153230.3(FBXO39):c.478A>G (p.Met160Val) rs1317799694 0.00001
NM_153230.3(FBXO39):c.519G>C (p.Arg173Ser) rs1468071224 0.00001
NM_153230.3(FBXO39):c.931A>G (p.Ile311Val) rs757022078 0.00001
NM_153230.3(FBXO39):c.1046A>T (p.Asn349Ile) rs1976577926
NM_153230.3(FBXO39):c.1049A>T (p.Asn350Ile)
NM_153230.3(FBXO39):c.1111T>C (p.Phe371Leu)
NM_153230.3(FBXO39):c.1184C>T (p.Ala395Val) rs2544764405
NM_153230.3(FBXO39):c.1247C>A (p.Thr416Asn)
NM_153230.3(FBXO39):c.1258A>G (p.Ile420Val) rs1415156164
NM_153230.3(FBXO39):c.1277A>C (p.Lys426Thr) rs2544764947
NM_153230.3(FBXO39):c.1285G>A (p.Glu429Lys) rs775055409
NM_153230.3(FBXO39):c.128G>A (p.Cys43Tyr) rs1487372888
NM_153230.3(FBXO39):c.1312G>A (p.Val438Ile)
NM_153230.3(FBXO39):c.151T>C (p.Tyr51His)
NM_153230.3(FBXO39):c.199C>T (p.Pro67Ser)
NM_153230.3(FBXO39):c.205A>G (p.Arg69Gly) rs2544760476
NM_153230.3(FBXO39):c.213T>G (p.His71Gln)
NM_153230.3(FBXO39):c.270G>T (p.Glu90Asp)
NM_153230.3(FBXO39):c.373C>T (p.Arg125Cys) rs889703951
NM_153230.3(FBXO39):c.391A>G (p.Ile131Val) rs1244209960
NM_153230.3(FBXO39):c.464T>G (p.Phe155Cys)
NM_153230.3(FBXO39):c.5A>G (p.Asp2Gly)
NM_153230.3(FBXO39):c.704G>C (p.Cys235Ser) rs2544760968
NM_153230.3(FBXO39):c.754C>T (p.Arg252Trp)
NM_153230.3(FBXO39):c.775C>T (p.His259Tyr)
NM_153230.3(FBXO39):c.791A>G (p.His264Arg) rs2544761067
NM_153230.3(FBXO39):c.7G>A (p.Glu3Lys)
NM_153230.3(FBXO39):c.941G>T (p.Arg314Ile)
NM_153230.3(FBXO39):c.944G>A (p.Ser315Asn) rs1311807573

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