ClinVar Miner

List of variants in gene FBXL4 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 120
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HGVS dbSNP gnomAD frequency
NM_001278716.2(FBXL4):c.1103+140T>C rs72627757 0.01653
NM_001278716.2(FBXL4):c.1103+29T>C rs189497833 0.01110
NM_001278716.2(FBXL4):c.1389+184G>A rs150045568 0.01103
NM_001278716.2(FBXL4):c.*90G>C rs111226417 0.00576
NM_001278716.2(FBXL4):c.978A>G (p.Gln326=) rs61744041 0.00506
NM_001278716.2(FBXL4):c.1317+264G>A rs141987023 0.00396
NM_001278716.2(FBXL4):c.1104-126T>A rs550657550 0.00376
NM_001278716.2(FBXL4):c.*9A>G rs185850413 0.00127
NM_001278716.2(FBXL4):c.-69A>G rs144837535 0.00112
NM_001278716.2(FBXL4):c.737T>C (p.Ile246Thr) rs143154211 0.00076
NM_001278716.2(FBXL4):c.65G>A (p.Arg22Gln) rs147696366 0.00057
NM_001278716.2(FBXL4):c.-79A>G rs574428980 0.00043
NM_001278716.2(FBXL4):c.1083C>T (p.Ile361=) rs368029297 0.00027
NM_001278716.2(FBXL4):c.79A>G (p.Thr27Ala) rs142853738 0.00024
NM_001278716.2(FBXL4):c.1073G>A (p.Arg358Lys) rs372544390 0.00021
NM_001278716.2(FBXL4):c.1317+19T>G rs201615847 0.00021
NM_001278716.2(FBXL4):c.541A>G (p.Thr181Ala) rs150748757 0.00021
NM_001278716.2(FBXL4):c.1723G>T (p.Ala575Ser) rs200435702 0.00019
NM_001278716.2(FBXL4):c.351G>A (p.Thr117=) rs375173811 0.00018
NM_001278716.2(FBXL4):c.1103+13C>T rs182076681 0.00016
NM_001278716.2(FBXL4):c.1209A>G (p.Leu403=) rs764546116 0.00012
NM_001278716.2(FBXL4):c.735T>C (p.Asp245=) rs369242693 0.00012
NM_001278716.2(FBXL4):c.1445G>A (p.Arg482Gln) rs200372976 0.00011
NM_001278716.2(FBXL4):c.1389+23T>C rs182295874 0.00010
NM_001278716.2(FBXL4):c.936G>A (p.Gln312=) rs142814111 0.00010
NM_001278716.2(FBXL4):c.300T>C (p.Tyr100=) rs573472397 0.00009
NM_001278716.2(FBXL4):c.1125C>T (p.Ser375=) rs377550308 0.00008
NM_001278716.2(FBXL4):c.1566C>T (p.Thr522=) rs149704398 0.00008
NM_001278716.2(FBXL4):c.813C>T (p.Leu271=) rs146999462 0.00008
NM_001278716.2(FBXL4):c.104A>G (p.His35Arg) rs201901274 0.00006
NM_001278716.2(FBXL4):c.78T>C (p.Ala26=) rs774610091 0.00006
NM_001278716.2(FBXL4):c.48T>C (p.Tyr16=) rs748705687 0.00005
NM_001278716.2(FBXL4):c.1318-16T>C rs768679543 0.00004
NM_001278716.2(FBXL4):c.9G>A (p.Pro3=) rs773041308 0.00004
NM_001278716.2(FBXL4):c.1104-19T>C rs765527736 0.00003
NM_001278716.2(FBXL4):c.1318-15G>C rs373175308 0.00003
NM_001278716.2(FBXL4):c.540T>G (p.Pro180=) rs760238524 0.00003
NM_001278716.2(FBXL4):c.714T>G (p.Thr238=) rs776419278 0.00003
NM_001278716.2(FBXL4):c.1056A>G (p.Leu352=) rs779748858 0.00002
NM_001278716.2(FBXL4):c.1464A>G (p.Arg488=) rs748404878 0.00002
NM_001278716.2(FBXL4):c.219T>C (p.Tyr73=) rs747536886 0.00002
NM_001278716.2(FBXL4):c.766G>A (p.Gly256Ser) rs765912815 0.00002
NM_001278716.2(FBXL4):c.1009C>T (p.Leu337=) rs778318524 0.00001
NM_001278716.2(FBXL4):c.1020A>G (p.Leu340=) rs747657121 0.00001
NM_001278716.2(FBXL4):c.1137C>T (p.Arg379=) rs895469467 0.00001
NM_001278716.2(FBXL4):c.135C>T (p.Ser45=) rs764057679 0.00001
NM_001278716.2(FBXL4):c.1389+13G>C rs768430744 0.00001
NM_001278716.2(FBXL4):c.1656T>C (p.Asp552=) rs779344587 0.00001
NM_001278716.2(FBXL4):c.1703-14T>C rs773834428 0.00001
NM_001278716.2(FBXL4):c.1764T>G (p.Ser588=) rs770326964 0.00001
NM_001278716.2(FBXL4):c.273T>C (p.Phe91=) rs1438963021 0.00001
NM_001278716.2(FBXL4):c.654T>C (p.Thr218=) rs1271495426 0.00001
NM_001278716.2(FBXL4):c.744T>C (p.Asp248=) rs149549442 0.00001
NM_001278716.2(FBXL4):c.906A>G (p.Arg302=) rs746193063 0.00001
NM_001278716.2(FBXL4):c.1103+13C>A rs182076681
NM_001278716.2(FBXL4):c.1103+13C>G rs182076681
NM_001278716.2(FBXL4):c.1103+14C>T
NM_001278716.2(FBXL4):c.1103+30del rs377101732
NM_001278716.2(FBXL4):c.1104-11T>C
NM_001278716.2(FBXL4):c.1104-15A>G
NM_001278716.2(FBXL4):c.1104-4G>T rs370992555
NM_001278716.2(FBXL4):c.1137C>G (p.Arg379=)
NM_001278716.2(FBXL4):c.114A>C (p.Ile38=)
NM_001278716.2(FBXL4):c.1167T>C (p.Asn389=) rs1322745455
NM_001278716.2(FBXL4):c.1200T>C (p.Cys400=)
NM_001278716.2(FBXL4):c.1224C>T (p.Leu408=)
NM_001278716.2(FBXL4):c.1303C>A (p.Arg435=)
NM_001278716.2(FBXL4):c.1317+13del
NM_001278716.2(FBXL4):c.1318-12C>G
NM_001278716.2(FBXL4):c.1318-18T>C
NM_001278716.2(FBXL4):c.1318-4G>T
NM_001278716.2(FBXL4):c.1362G>A (p.Gln454=)
NM_001278716.2(FBXL4):c.1389+11G>A rs1770815162
NM_001278716.2(FBXL4):c.1390-4C>G
NM_001278716.2(FBXL4):c.1431G>A (p.Lys477=) rs1582359691
NM_001278716.2(FBXL4):c.1443C>A (p.Leu481=) rs1168654660
NM_001278716.2(FBXL4):c.1452G>A (p.Leu484=)
NM_001278716.2(FBXL4):c.1497A>G (p.Glu499=)
NM_001278716.2(FBXL4):c.1518A>G (p.Leu506=) rs556881504
NM_001278716.2(FBXL4):c.1587A>G (p.Ala529=) rs1582359148
NM_001278716.2(FBXL4):c.1699T>C (p.Leu567=) rs183776114
NM_001278716.2(FBXL4):c.1702+11A>T rs369407577
NM_001278716.2(FBXL4):c.1702+14A>G
NM_001278716.2(FBXL4):c.1702+18A>G rs776605924
NM_001278716.2(FBXL4):c.1703-36TGTTT[3]
NM_001278716.2(FBXL4):c.1703-36TGTTT[4]
NM_001278716.2(FBXL4):c.1703-36TGTTT[6] rs377666976
NM_001278716.2(FBXL4):c.1703-5A>C
NM_001278716.2(FBXL4):c.1704A>G (p.Gly568=)
NM_001278716.2(FBXL4):c.1716A>G (p.Val572=)
NM_001278716.2(FBXL4):c.1788G>A (p.Ser596=) rs745713189
NM_001278716.2(FBXL4):c.192T>C (p.His64=)
NM_001278716.2(FBXL4):c.207T>C (p.Asn69=)
NM_001278716.2(FBXL4):c.249T>C (p.Asn83=) rs372346466
NM_001278716.2(FBXL4):c.255C>T (p.Phe85=)
NM_001278716.2(FBXL4):c.36C>G (p.Thr12=) rs749635212
NM_001278716.2(FBXL4):c.36C>T (p.Thr12=)
NM_001278716.2(FBXL4):c.444C>T (p.Pro148=)
NM_001278716.2(FBXL4):c.447A>G (p.Gly149=)
NM_001278716.2(FBXL4):c.456T>C (p.Ile152=)
NM_001278716.2(FBXL4):c.513-13C>G rs200592647
NM_001278716.2(FBXL4):c.513-13C>T
NM_001278716.2(FBXL4):c.561A>G (p.Gln187=)
NM_001278716.2(FBXL4):c.639T>C (p.Leu213=)
NM_001278716.2(FBXL4):c.666A>C (p.Ala222=) rs781455701
NM_001278716.2(FBXL4):c.666A>G (p.Ala222=)
NM_001278716.2(FBXL4):c.702T>C (p.Leu234=) rs1554221171
NM_001278716.2(FBXL4):c.738A>T (p.Ile246=)
NM_001278716.2(FBXL4):c.747T>A (p.Asp249Glu) rs138206466
NM_001278716.2(FBXL4):c.759A>G (p.Glu253=)
NM_001278716.2(FBXL4):c.75A>G (p.Thr25=)
NM_001278716.2(FBXL4):c.807T>C (p.Ala269=)
NM_001278716.2(FBXL4):c.813C>A (p.Leu271=)
NM_001278716.2(FBXL4):c.858+12A>C
NM_001278716.2(FBXL4):c.858+7C>G
NM_001278716.2(FBXL4):c.858+9A>G
NM_001278716.2(FBXL4):c.951T>C (p.Pro317=)
NM_001278716.2(FBXL4):c.952C>T (p.Leu318=)
NM_001278716.2(FBXL4):c.954G>A (p.Leu318=) rs762811521
NM_001278716.2(FBXL4):c.9G>C (p.Pro3=) rs773041308

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