ClinVar Miner

List of variants in gene FBXL8

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_018378.3(FBXL8):c.601G>C (p.Ala201Pro) rs200489971 0.00017
NM_018378.3(FBXL8):c.611C>T (p.Ser204Leu) rs372385276 0.00012
NM_018378.3(FBXL8):c.313G>A (p.Gly105Ser) rs753145061 0.00008
NM_018378.3(FBXL8):c.10C>G (p.Pro4Ala) rs113936384 0.00007
NM_018378.3(FBXL8):c.130G>A (p.Val44Met) rs372208643 0.00007
NM_018378.3(FBXL8):c.367G>A (p.Val123Ile) rs982262551 0.00007
NM_018378.3(FBXL8):c.577C>G (p.Leu193Val) rs369684413 0.00007
NM_018378.3(FBXL8):c.598C>G (p.Leu200Val) rs373307693 0.00005
NM_018378.3(FBXL8):c.160T>C (p.Cys54Arg) rs2030965554 0.00003
NM_018378.3(FBXL8):c.657C>A (p.Phe219Leu) rs560299174 0.00003
NM_018378.3(FBXL8):c.302C>T (p.Pro101Leu) rs1401056929 0.00001
NM_018378.3(FBXL8):c.428G>A (p.Arg143Gln) rs759079197 0.00001
NM_018378.3(FBXL8):c.467A>C (p.Gln156Pro) rs1396705325 0.00001
NM_018378.3(FBXL8):c.1027G>C (p.Val343Leu) rs1014290681
NM_018378.3(FBXL8):c.116C>T (p.Ala39Val)
NM_018378.3(FBXL8):c.184C>T (p.Pro62Ser)
NM_018378.3(FBXL8):c.219C>A (p.Asn73Lys)
NM_018378.3(FBXL8):c.263C>A (p.Ala88Glu) rs2506992456
NM_018378.3(FBXL8):c.437C>T (p.Ser146Phe)
NM_018378.3(FBXL8):c.452A>G (p.Asp151Gly)
NM_018378.3(FBXL8):c.453C>A (p.Asp151Glu)
NM_018378.3(FBXL8):c.454G>C (p.Ala152Pro)
NM_018378.3(FBXL8):c.514A>G (p.Ser172Gly)
NM_018378.3(FBXL8):c.538C>A (p.Pro180Thr)
NM_018378.3(FBXL8):c.538C>G (p.Pro180Ala) rs148684911
NM_018378.3(FBXL8):c.538C>T (p.Pro180Ser)
NM_018378.3(FBXL8):c.58C>G (p.Leu20Val) rs150449492
NM_018378.3(FBXL8):c.653C>T (p.Pro218Leu) rs1366316106
NM_018378.3(FBXL8):c.665T>C (p.Leu222Ser)
NM_018378.3(FBXL8):c.682T>G (p.Cys228Gly) rs2506994305
NM_018378.3(FBXL8):c.736C>G (p.Arg246Gly)
NM_018378.3(FBXL8):c.746A>G (p.His249Arg) rs955544836
NM_018378.3(FBXL8):c.758C>G (p.Ala253Gly)
NM_018378.3(FBXL8):c.769G>C (p.Glu257Gln)
NM_018378.3(FBXL8):c.782C>A (p.Ala261Glu) rs759949823
NM_018378.3(FBXL8):c.790G>A (p.Ala264Thr)
NM_018378.3(FBXL8):c.806G>A (p.Arg269His) rs2506994937
NM_018378.3(FBXL8):c.878G>A (p.Arg293His)
NM_018378.3(FBXL8):c.905C>T (p.Thr302Ile) rs776855884
NM_018378.3(FBXL8):c.919G>A (p.Glu307Lys)
NM_018378.3(FBXL8):c.964G>C (p.Glu322Gln)

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