ClinVar Miner

List of variants in gene CUL3 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP gnomAD frequency
NM_003590.5(CUL3):c.-201C>G rs188890085 0.00738
NM_003590.5(CUL3):c.*3665T>A rs374191606 0.00230
NM_003590.5(CUL3):c.*2130A>G rs555995940 0.00154
NM_003590.5(CUL3):c.*2272T>C rs556914502 0.00132
NM_003590.5(CUL3):c.*3753T>C rs558805673 0.00068
NM_003590.5(CUL3):c.*294A>G rs532967850 0.00067
NM_003590.5(CUL3):c.*3026G>A rs748865811 0.00034
NM_003590.5(CUL3):c.-270G>A rs913597782 0.00029
NM_003590.5(CUL3):c.*89A>T rs192166927 0.00022
NM_003590.5(CUL3):c.*1506G>A rs886055691 0.00019
NM_003590.5(CUL3):c.*2341G>C rs938971844 0.00014
NM_003590.5(CUL3):c.*3596A>G rs764772276 0.00014
NM_003590.5(CUL3):c.*2766G>C rs747359530 0.00013
NM_003590.5(CUL3):c.*4088T>C rs556849083 0.00013
NM_003590.5(CUL3):c.*3810C>T rs940993118 0.00009
NM_003590.5(CUL3):c.*664T>G rs778642011 0.00009
NM_003590.5(CUL3):c.*915A>G rs760530227 0.00007
NM_003590.5(CUL3):c.*1883T>C rs190478338 0.00006
NM_003590.5(CUL3):c.*2195A>G rs886055688 0.00006
NM_003590.5(CUL3):c.*2756G>A rs886055684 0.00006
NM_003590.5(CUL3):c.-169C>T rs1355759034 0.00006
NM_003590.5(CUL3):c.*2008G>T rs185186023 0.00004
NM_003590.5(CUL3):c.*2469G>C rs886055686 0.00004
NM_003590.5(CUL3):c.*3392A>G rs886055680 0.00004
NM_003590.5(CUL3):c.*782G>T rs926333413 0.00004
NM_003590.5(CUL3):c.*2553A>G rs1440895219 0.00003
NM_003590.5(CUL3):c.*2854A>G rs772430576 0.00003
NM_003590.5(CUL3):c.*2868T>C rs886055683 0.00003
NM_003590.5(CUL3):c.*2689T>C rs1248975644 0.00002
NM_003590.5(CUL3):c.*3134A>T rs552216335 0.00002
NM_003590.5(CUL3):c.*2093A>G rs886055689 0.00001
NM_003590.5(CUL3):c.*3766G>A rs886055679 0.00001
NM_003590.5(CUL3):c.*3958C>T rs1691077506 0.00001
NM_003590.5(CUL3):c.*496A>T rs1691214384 0.00001
NM_003590.5(CUL3):c.*540G>A rs1407928300 0.00001
NM_003590.5(CUL3):c.*790T>G rs980398909 0.00001
NM_003590.5(CUL3):c.*84C>T rs968196250 0.00001
NM_003590.5(CUL3):c.*905A>G rs764172604 0.00001
NM_003590.5(CUL3):c.1036T>C (p.Leu346=) rs758182990 0.00001
NM_003590.5(CUL3):c.1293T>C (p.Tyr431=) rs767137215 0.00001
NM_003590.5(CUL3):c.*1451AAC[1] rs756120079
NM_003590.5(CUL3):c.*1498C>G rs886055692
NM_003590.5(CUL3):c.*1518A>T rs886055690
NM_003590.5(CUL3):c.*1943A>T rs890153682
NM_003590.5(CUL3):c.*2037del rs770315174
NM_003590.5(CUL3):c.*207G>A rs886055694
NM_003590.5(CUL3):c.*2424C>T rs886055687
NM_003590.5(CUL3):c.*2584T>C rs886055685
NM_003590.5(CUL3):c.*2851A>C rs1691124781
NM_003590.5(CUL3):c.*2946_*2949del rs886055682
NM_003590.5(CUL3):c.*3096G>C rs886055681
NM_003590.5(CUL3):c.*3785dup rs886055678
NM_003590.5(CUL3):c.*3922A>G rs1691078689
NM_003590.5(CUL3):c.*499T>C rs1691214301
NM_003590.5(CUL3):c.*527A>G rs1171555841
NM_003590.5(CUL3):c.*545A>G rs886055693
NM_003590.5(CUL3):c.*736A>G rs531395316
NM_003590.5(CUL3):c.*784G>A rs1224616813
NM_003590.5(CUL3):c.-118C>G rs1695550733
NM_003590.5(CUL3):c.-143G>C rs556768798
NM_003590.5(CUL3):c.-173G>C rs183605797
NM_003590.5(CUL3):c.-185G>C rs1232933028
NM_003590.5(CUL3):c.-246C>T rs928887003
NM_003590.5(CUL3):c.-291A>T rs1695560106
NM_003590.5(CUL3):c.-317C>A rs950809352
NM_003590.5(CUL3):c.1028A>G (p.Gln343Arg) rs1692622022
NM_003590.5(CUL3):c.1462A>C (p.Arg488=) rs1692449966
NM_003590.5(CUL3):c.1609A>G (p.Arg537Gly)
NM_003590.5(CUL3):c.2102A>T (p.His701Leu) rs886055695
NM_003590.5(CUL3):c.304C>A (p.Leu102Ile) rs886055697
NM_003590.5(CUL3):c.310A>T (p.Thr104Ser) rs886055696
NM_003590.5(CUL3):c.884-5T>C rs1692626427

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