ClinVar Miner

List of variants in gene FBXO38 reported by GeneDx

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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_205836.3(FBXO38):c.730+254C>G rs4639213 0.42508
NM_205836.3(FBXO38):c.2654-86T>G rs6861078 0.42302
NM_205836.3(FBXO38):c.1619-4G>T rs11168047 0.42278
NM_205836.3(FBXO38):c.1094-293A>G rs7728004 0.42201
NM_205836.3(FBXO38):c.3170+11T>C rs10051223 0.42131
NM_205836.3(FBXO38):c.426+24T>G rs34685718 0.28191
NM_205836.3(FBXO38):c.1774T>C (p.Ser592Pro) rs10043775 0.27167
NM_205836.3(FBXO38):c.3171-284G>T rs10056586 0.27075
NM_205836.3(FBXO38):c.3274+255G>A rs9325097 0.27074
NM_205836.3(FBXO38):c.3389-63C>T rs3734120 0.26380
NM_205836.3(FBXO38):c.128+195T>G rs10072051 0.25113
NM_205836.3(FBXO38):c.869-249T>C rs4349707 0.24962
NM_205836.3(FBXO38):c.1264+102G>A rs12717973 0.20624
NM_205836.3(FBXO38):c.962+18A>G rs10077690 0.20380
NM_205836.3(FBXO38):c.128+239T>G rs11957411 0.15147
NM_205836.3(FBXO38):c.1408-203G>A rs59691479 0.07492
NM_205836.3(FBXO38):c.*118A>G rs75666198 0.05820
NM_205836.3(FBXO38):c.2654-189T>G rs11959865 0.03263
NM_205836.3(FBXO38):c.262+223G>A rs76852156 0.03260
NM_205836.3(FBXO38):c.2680G>A (p.Ala894Thr) rs11949133 0.03254
NM_205836.3(FBXO38):c.868+42A>G rs79846164 0.03031
NM_205836.3(FBXO38):c.731-226C>T rs74941890 0.02943
NM_205836.3(FBXO38):c.1619-115G>A rs114696037 0.02283
NM_205836.3(FBXO38):c.2654-16T>C rs147707335 0.02178
NM_205836.3(FBXO38):c.731-57G>A rs115335406 0.01973
NM_205836.3(FBXO38):c.3274+218A>G rs74487325 0.01852
NM_205836.3(FBXO38):c.3171-271T>G rs59722938 0.01842
NM_205836.3(FBXO38):c.198A>G (p.Leu66=) rs74863106 0.01749
NM_205836.3(FBXO38):c.1738+64A>G rs10068442 0.01003
NM_205836.3(FBXO38):c.1264+214A>T rs151111063 0.00927
NM_205836.3(FBXO38):c.962+132C>T rs10070268 0.00920
NM_205836.3(FBXO38):c.1408-25C>T rs111661850 0.00918
NM_205836.3(FBXO38):c.869-101T>C rs10045756 0.00918
NM_205836.3(FBXO38):c.868+105G>A rs116413316 0.00720
NM_205836.3(FBXO38):c.3275-31G>A rs138926886 0.00718
NM_205836.3(FBXO38):c.868+212A>G rs6878613 0.00651
NM_205836.3(FBXO38):c.129-66A>G rs114174259 0.00645
NM_205836.3(FBXO38):c.593-236A>G rs115425944 0.00583
NM_205836.3(FBXO38):c.593-13A>T rs61555444 0.00559
NM_205836.3(FBXO38):c.3024+265A>G rs185100825 0.00521
NM_205836.3(FBXO38):c.263-319A>G rs77866609 0.00436
NM_205836.3(FBXO38):c.2857+24A>G rs6861453 0.00386
NM_205836.3(FBXO38):c.592+177G>C rs190963429 0.00385
NM_205836.3(FBXO38):c.1408-108C>G rs192062226 0.00342
NM_205836.3(FBXO38):c.87T>C (p.Tyr29=) rs77480566 0.00254
NM_205836.3(FBXO38):c.2341C>T (p.Pro781Ser) rs116266000 0.00134
NM_205836.3(FBXO38):c.2146A>G (p.Ser716Gly) rs150893158 0.00050
NM_205836.3(FBXO38):c.2889G>C (p.Lys963Asn) rs371555180 0.00039
NM_205836.3(FBXO38):c.1861C>T (p.Arg621Cys) rs146121161 0.00017
NM_205836.3(FBXO38):c.1394G>A (p.Arg465His) rs200187682 0.00010
NM_205836.3(FBXO38):c.2231T>C (p.Val744Ala) rs372364064 0.00009
NM_205836.3(FBXO38):c.3439A>G (p.Met1147Val) rs550138374 0.00003
NM_205836.3(FBXO38):c.2234A>T (p.Asp745Val) rs145266253 0.00002
NM_205836.3(FBXO38):c.2203G>A (p.Gly735Ser) rs779561720 0.00001
NM_205836.3(FBXO38):c.3024+6G>A rs146510581 0.00001
NM_205836.3(FBXO38):c.1202G>C (p.Cys401Ser) rs777938088
NM_205836.3(FBXO38):c.129-310dup rs200385007
NM_205836.3(FBXO38):c.1407+78_1407+79dup rs376168098
NM_205836.3(FBXO38):c.1407+79del rs376168098
NM_205836.3(FBXO38):c.1407+79dup rs376168098
NM_205836.3(FBXO38):c.1408-24G>C rs58313354
NM_205836.3(FBXO38):c.1487A>G (p.Asn496Ser) rs1315072548
NM_205836.3(FBXO38):c.1526A>G (p.His509Arg)
NM_205836.3(FBXO38):c.1895C>G (p.Ser632Ter)
NM_205836.3(FBXO38):c.2050G>A (p.Asp684Asn)
NM_205836.3(FBXO38):c.2112_2113del (p.Cys704fs)
NM_205836.3(FBXO38):c.2164T>C (p.Ser722Pro) rs1168710534
NM_205836.3(FBXO38):c.2654-90T>G rs114474976
NM_205836.3(FBXO38):c.3274+117G>A rs3734121
NM_205836.3(FBXO38):c.3274+146C>T rs78155568
NM_205836.3(FBXO38):c.3553G>A (p.Asp1185Asn)
NM_205836.3(FBXO38):c.455T>C (p.Val152Ala)
NM_205836.3(FBXO38):c.712G>A (p.Val238Ile) rs144890577
NM_205836.3(FBXO38):c.730+207dup rs764926425
NM_205836.3(FBXO38):c.757C>T (p.Pro253Ser)
NM_205836.3(FBXO38):c.914A>G (p.Asn305Ser)

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