ClinVar Miner

List of variants in gene CUL3 reported as uncertain significance by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_003590.5(CUL3):c.137G>A (p.Arg46His) rs190453078 0.00006
NM_003590.5(CUL3):c.1061G>A (p.Arg354His) rs983814335 0.00001
NM_003590.5(CUL3):c.1108A>C (p.Ile370Leu) rs1445122491 0.00001
NM_003590.5(CUL3):c.2092G>A (p.Asp698Asn) rs371342121 0.00001
NM_003590.5(CUL3):c.415G>A (p.Val139Ile) rs1692972942 0.00001
NM_003590.5(CUL3):c.458G>A (p.Arg153His) rs972626651 0.00001
NM_003590.5(CUL3):c.620C>T (p.Ala207Val) rs750610847 0.00001
NM_003590.5(CUL3):c.622C>A (p.Pro208Thr) rs1365715412 0.00001
NM_003590.5(CUL3):c.799G>C (p.Glu267Gln) rs757584952 0.00001
NM_003590.5(CUL3):c.826A>G (p.Ile276Val) rs1465086578 0.00001
NM_003590.5(CUL3):c.908T>G (p.Phe303Cys) rs996315289 0.00001
NC_000002.11:g.(?_225400225)_(225400378_?)del
NM_003590.5(CUL3):c.1024A>G (p.Ile342Val) rs1692622223
NM_003590.5(CUL3):c.1030-8T>G
NM_003590.5(CUL3):c.1043T>C (p.Leu348Pro) rs2106203843
NM_003590.5(CUL3):c.1057G>A (p.Asp353Asn)
NM_003590.5(CUL3):c.1058A>C (p.Asp353Ala) rs1189209020
NM_003590.5(CUL3):c.1070T>G (p.Leu357Arg) rs754587052
NM_003590.5(CUL3):c.115A>C (p.Asn39His) rs2469185181
NM_003590.5(CUL3):c.1206+3_1206+4insTAC rs2469980677
NM_003590.5(CUL3):c.1207-5T>G rs199469652
NM_003590.5(CUL3):c.1243G>A (p.Ala415Thr)
NM_003590.5(CUL3):c.1252C>T (p.Leu418Phe)
NM_003590.5(CUL3):c.1264A>C (p.Met422Leu) rs2469974774
NM_003590.5(CUL3):c.1306T>G (p.Leu436Val) rs2106196965
NM_003590.5(CUL3):c.1377+6G>T
NM_003590.5(CUL3):c.1450A>G (p.Met484Val) rs1692450392
NM_003590.5(CUL3):c.1486-3T>C
NM_003590.5(CUL3):c.1568A>G (p.Asn523Ser)
NM_003590.5(CUL3):c.1585A>G (p.Arg529Gly)
NM_003590.5(CUL3):c.1588C>T (p.His530Tyr)
NM_003590.5(CUL3):c.1592C>T (p.Ala531Val)
NM_003590.5(CUL3):c.1609A>G (p.Arg537Gly) rs2469964203
NM_003590.5(CUL3):c.1610+10A>G
NM_003590.5(CUL3):c.1610+4A>G
NM_003590.5(CUL3):c.1637G>A (p.Arg546Gln) rs770136825
NM_003590.5(CUL3):c.1640A>C (p.Gln547Pro) rs2469957258
NM_003590.5(CUL3):c.1707+5del
NM_003590.5(CUL3):c.1754C>G (p.Ser585Cys) rs2106180071
NM_003590.5(CUL3):c.1808T>C (p.Met603Thr) rs200435739
NM_003590.5(CUL3):c.1823G>A (p.Arg608Lys) rs2106179600
NM_003590.5(CUL3):c.1831T>A (p.Tyr611Asn)
NM_003590.5(CUL3):c.2029+4T>C
NM_003590.5(CUL3):c.2030-3T>C rs1394913111
NM_003590.5(CUL3):c.2033C>T (p.Ala678Val) rs2106143643
NM_003590.5(CUL3):c.2089G>A (p.Asp697Asn)
NM_003590.5(CUL3):c.2138C>G (p.Ser713Cys) rs2106142737
NM_003590.5(CUL3):c.2187G>C (p.Gln729His)
NM_003590.5(CUL3):c.2195C>T (p.Ala732Val) rs745316138
NM_003590.5(CUL3):c.2231G>A (p.Arg744His) rs2106133454
NM_003590.5(CUL3):c.227G>C (p.Gly76Ala) rs2106304242
NM_003590.5(CUL3):c.2281C>T (p.Arg761Cys) rs759758641
NM_003590.5(CUL3):c.2285A>G (p.Lys762Arg) rs761790580
NM_003590.5(CUL3):c.419A>G (p.Tyr140Cys) rs2470004152
NM_003590.5(CUL3):c.443G>A (p.Arg148Gln) rs2106223657
NM_003590.5(CUL3):c.539+5A>G rs2470003645
NM_003590.5(CUL3):c.606AGA[1] (p.Glu203del) rs770645060
NM_003590.5(CUL3):c.610G>A (p.Asp204Asn) rs1411316058
NM_003590.5(CUL3):c.679G>A (p.Glu227Lys)
NM_003590.5(CUL3):c.76G>T (p.Asp26Tyr) rs2106305184
NM_003590.5(CUL3):c.827T>C (p.Ile276Thr)
NM_003590.5(CUL3):c.857A>C (p.His286Pro)
NM_003590.5(CUL3):c.883+3_883+6del rs2469994698
NM_003590.5(CUL3):c.932A>G (p.Lys311Arg) rs2469984576
NM_003590.5(CUL3):c.946T>C (p.Cys316Arg)
NM_003590.5(CUL3):c.992AAG[1] (p.Glu332del) rs1472792526

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