ClinVar Miner

List of variants in gene CUBN reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP gnomAD frequency
NM_001081.4(CUBN):c.2756A>G (p.His919Arg) rs148869805 0.00464
NM_001081.4(CUBN):c.6125-2A>G rs75386064 0.00226
NM_001081.4(CUBN):c.10119C>A (p.Val3373=) rs139596037 0.00168
NM_001081.4(CUBN):c.5069C>T (p.Ala1690Val) rs141640975 0.00155
NM_001081.4(CUBN):c.8894T>C (p.Phe2965Ser) rs117620008 0.00133
NM_001081.4(CUBN):c.6673G>C (p.Asp2225His) rs140862613 0.00111
NM_001081.4(CUBN):c.3356T>C (p.Leu1119Ser) rs141164907 0.00089
NM_001081.4(CUBN):c.10105A>G (p.Ser3369Gly) rs145023719 0.00070
NM_001081.4(CUBN):c.8399C>T (p.Thr2800Ile) rs141737312 0.00070
NM_001081.4(CUBN):c.4669C>T (p.Leu1557Phe) rs140970422 0.00064
NM_001081.4(CUBN):c.9236+8A>G rs372673718 0.00038
NM_001081.4(CUBN):c.8593G>A (p.Val2865Met) rs146847375 0.00037
NM_001081.4(CUBN):c.6091A>G (p.Thr2031Ala) rs150392211 0.00034
NM_001081.4(CUBN):c.7837A>C (p.Ile2613Leu) rs144626884 0.00031
NM_001081.4(CUBN):c.10834C>T (p.Arg3612Trp) rs151134377 0.00029
NM_001081.4(CUBN):c.6263T>C (p.Phe2088Ser) rs74844886 0.00029
NM_001081.4(CUBN):c.814G>A (p.Gly272Arg) rs146035059 0.00029
NM_001081.4(CUBN):c.3646C>G (p.Pro1216Ala) rs145881708 0.00027
NM_001081.4(CUBN):c.6560C>T (p.Ser2187Leu) rs143899993 0.00026
NM_001081.4(CUBN):c.9079G>A (p.Gly3027Arg) rs150202444 0.00021
NM_001081.4(CUBN):c.5926+5G>A rs143301088 0.00019
NM_001081.4(CUBN):c.6020C>T (p.Thr2007Met) rs140202552 0.00019
NM_001081.4(CUBN):c.6479A>G (p.Asp2160Gly) rs144704318 0.00019
NM_001081.4(CUBN):c.3995A>G (p.Asn1332Ser) rs370803308 0.00017
NM_001081.4(CUBN):c.7906C>T (p.Arg2636Ter) rs137998687 0.00016
NM_001081.4(CUBN):c.427A>C (p.Asn143His) rs151018922 0.00015
NM_001081.4(CUBN):c.1450A>G (p.Ser484Gly) rs750735519 0.00014
NM_001081.4(CUBN):c.9418G>A (p.Ala3140Thr) rs148491916 0.00014
NM_001081.4(CUBN):c.4639C>T (p.Arg1547Cys) rs375920680 0.00013
NM_001081.4(CUBN):c.5459A>G (p.Tyr1820Cys) rs139369652 0.00013
NM_001081.4(CUBN):c.2738G>C (p.Ser913Thr) rs201589187 0.00012
NM_001081.4(CUBN):c.6661G>A (p.Val2221Ile) rs143291127 0.00011
NM_001081.4(CUBN):c.10641G>A (p.Arg3547=) rs145909413 0.00010
NM_001081.4(CUBN):c.323G>A (p.Ser108Asn) rs543983858 0.00010
NM_001081.4(CUBN):c.3746G>A (p.Arg1249His) rs151039810 0.00010
NM_001081.4(CUBN):c.5323C>T (p.Arg1775Trp) rs1276708 0.00010
NM_001081.4(CUBN):c.6268A>G (p.Lys2090Glu) rs201374966 0.00010
NM_001081.4(CUBN):c.6613G>A (p.Gly2205Arg) rs140883483 0.00008
NM_001081.4(CUBN):c.8765G>A (p.Ser2922Asn) rs777692110 0.00008
NM_001081.4(CUBN):c.1010C>T (p.Pro337Leu) rs202153130 0.00007
NM_001081.4(CUBN):c.3391A>G (p.Thr1131Ala) rs201138390 0.00007
NM_001081.4(CUBN):c.5084G>A (p.Arg1695His) rs145880377 0.00006
NM_001081.4(CUBN):c.7400A>G (p.Asn2467Ser) rs200197243 0.00006
NM_001081.4(CUBN):c.10102A>G (p.Met3368Val) rs767333853 0.00005
NM_001081.4(CUBN):c.3496G>A (p.Gly1166Arg) rs201443885 0.00004
NM_001081.4(CUBN):c.5957A>T (p.Asp1986Val) rs772570411 0.00004
NM_001081.4(CUBN):c.2863G>A (p.Gly955Ser) rs567450170 0.00003
NM_001081.4(CUBN):c.6095G>A (p.Cys2032Tyr) rs201720797 0.00003
NM_001081.4(CUBN):c.736G>A (p.Val246Ile) rs760990753 0.00003
NM_001081.4(CUBN):c.10277C>G (p.Thr3426Arg) rs143066121 0.00001
NM_001081.4(CUBN):c.2418A>T (p.Lys806Asn) rs764656350 0.00001
NM_001081.4(CUBN):c.4268C>T (p.Thr1423Met) rs483352704 0.00001
NM_001081.4(CUBN):c.7342A>G (p.Ser2448Gly) rs776447439 0.00001
NM_001081.4(CUBN):c.7568T>C (p.Leu2523Pro) rs145347743 0.00001
NM_001081.4(CUBN):c.8908C>T (p.Arg2970Cys) rs562374248 0.00001
NM_001081.4(CUBN):c.10192_10193del (p.Asp3398fs) rs1564376600
NM_001081.4(CUBN):c.1030G>A (p.Gly344Arg)
NM_001081.4(CUBN):c.10431_10447del (p.Pro3477_Val3478insTer) rs1564374451
NM_001081.4(CUBN):c.10729G>T (p.Ala3577Ser) rs139051724
NM_001081.4(CUBN):c.1097G>C (p.Cys366Ser) rs1564518870
NM_001081.4(CUBN):c.2144C>T (p.Pro715Leu)
NM_001081.4(CUBN):c.2866A>G (p.Ile956Val)
NM_001081.4(CUBN):c.349-6T>A
NM_001081.4(CUBN):c.3649A>G (p.Asn1217Asp)
NM_001081.4(CUBN):c.4069C>G (p.Pro1357Ala) rs780012075
NM_001081.4(CUBN):c.4148A>G (p.Gln1383Arg)
NM_001081.4(CUBN):c.4299C>T (p.Ile1433=)
NM_001081.4(CUBN):c.4472A>C (p.Asp1491Ala) rs1064795523
NM_001081.4(CUBN):c.4656C>T (p.Phe1552=) rs2131697240
NM_001081.4(CUBN):c.4720A>G (p.Met1574Val) rs1482983523
NM_001081.4(CUBN):c.4759G>A (p.Ala1587Thr)
NM_001081.4(CUBN):c.4787G>A (p.Ser1596Asn) rs368081631
NM_001081.4(CUBN):c.4838G>T (p.Arg1613Leu)
NM_001081.4(CUBN):c.5056G>A (p.Gly1686Ser)
NM_001081.4(CUBN):c.5062G>A (p.Glu1688Lys)
NM_001081.4(CUBN):c.557A>G (p.Asn186Ser) rs1286216349
NM_001081.4(CUBN):c.5762G>A (p.Arg1921His)
NM_001081.4(CUBN):c.5840C>A (p.Ser1947Tyr) rs147617753
NM_001081.4(CUBN):c.5856_5858delinsGGC (p.Gly1953Ala) rs1564434486
NM_001081.4(CUBN):c.5965G>A (p.Val1989Met) rs368951850
NM_001081.4(CUBN):c.6398A>G (p.His2133Arg)
NM_001081.4(CUBN):c.6443A>G (p.Asn2148Ser)
NM_001081.4(CUBN):c.6497T>C (p.Leu2166Ser)
NM_001081.4(CUBN):c.6538G>A (p.Ala2180Thr) rs769495257
NM_001081.4(CUBN):c.6764C>T (p.Pro2255Leu)
NM_001081.4(CUBN):c.6916T>C (p.Trp2306Arg)
NM_001081.4(CUBN):c.7088G>C (p.Cys2363Ser) rs2131458198
NM_001081.4(CUBN):c.7661_7662inv (p.Pro2554Leu)
NM_001081.4(CUBN):c.7968_7969delinsTGTTATACCTTATATAA (p.Leu2656_Pro2657delinsPheValIleProTyrIleThr) rs2131430377
NM_001081.4(CUBN):c.8007dup (p.Val2670fs) rs1564414648
NM_001081.4(CUBN):c.8104del (p.Ser2702fs) rs1564412484
NM_001081.4(CUBN):c.8284C>A (p.Gln2762Lys) rs2131420598
NM_001081.4(CUBN):c.8290T>C (p.Cys2764Arg)
NM_001081.4(CUBN):c.8693T>A (p.Phe2898Tyr)
NM_001081.4(CUBN):c.9199A>G (p.Thr3067Ala)
NM_001081.4(CUBN):c.9266CCT[3] (p.Ser3090dup) rs1300066453
NM_001081.4(CUBN):c.9667T>C (p.Tyr3223His)

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