ClinVar Miner

List of variants in gene CUL7 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_014780.5(CUL7):c.2439A>G (p.Gln813=) rs9394939 0.97892
NM_014780.5(CUL7):c.2438A>G (p.Gln813Arg) rs9381231 0.97891
NM_014780.5(CUL7):c.3993G>A (p.Leu1331=) rs2273917 0.27596
NM_014780.5(CUL7):c.339C>T (p.Asp113=) rs4711738 0.22523
NM_014780.5(CUL7):c.4463T>C (p.Leu1488Pro) rs41274912 0.00688
NM_014780.5(CUL7):c.2614G>A (p.Gly872Ser) rs61750320 0.00170
NM_014780.5(CUL7):c.3049G>A (p.Ala1017Thr) rs34916226 0.00156
NM_014780.5(CUL7):c.861G>A (p.Gly287=) rs61750322 0.00140
NM_014780.5(CUL7):c.1859C>T (p.Pro620Leu) rs147326417 0.00115
NM_014780.5(CUL7):c.1067G>A (p.Arg356His) rs146227929 0.00114
NM_014780.5(CUL7):c.3768C>T (p.Ser1256=) rs138763036 0.00111
NM_014780.5(CUL7):c.4659G>A (p.Glu1553=) rs139243761 0.00107
NM_014780.5(CUL7):c.2115C>T (p.His705=) rs143128153 0.00098
NM_014780.5(CUL7):c.3695G>A (p.Arg1232Gln) rs36004037 0.00089
NM_014780.5(CUL7):c.1982G>A (p.Arg661Gln) rs139887350 0.00068
NM_014780.5(CUL7):c.4104G>A (p.Ala1368=) rs143333013 0.00065
NM_014780.5(CUL7):c.3876C>T (p.Ile1292=) rs147056081 0.00046
NM_014780.5(CUL7):c.4731C>T (p.Ala1577=) rs141716467 0.00038
NM_014780.5(CUL7):c.3432G>A (p.Thr1144=) rs144556973 0.00036
NM_014780.5(CUL7):c.687G>A (p.Thr229=) rs192945321 0.00019
NM_014780.5(CUL7):c.1570-8G>A rs372757013 0.00017
NM_014780.5(CUL7):c.4431C>T (p.Asn1477=) rs149530175 0.00011
NM_014780.5(CUL7):c.2064-5C>T rs115073371 0.00009
NM_014780.5(CUL7):c.426C>T (p.His142=) rs138730481 0.00008
NM_014780.5(CUL7):c.2603A>G (p.Asn868Ser) rs149360738 0.00007
NM_014780.5(CUL7):c.3747G>A (p.Leu1249=) rs141211365 0.00006
NM_014780.5(CUL7):c.1590A>C (p.Leu530=) rs552325363 0.00003
NM_014780.5(CUL7):c.2064-7C>T rs771693083 0.00003
NM_014780.5(CUL7):c.4059C>T (p.Ser1353=) rs748157885 0.00002
NM_014780.5(CUL7):c.1168GAG[1] (p.Glu391del) rs372224208
NM_014780.5(CUL7):c.123T>C (p.Arg41=)
NM_014780.5(CUL7):c.1782G>A (p.Ala594=) rs369092411
NM_014780.5(CUL7):c.1782G>C (p.Ala594=) rs369092411
NM_014780.5(CUL7):c.2438_2439delinsGG (p.Gln813Arg) rs61748654
NM_014780.5(CUL7):c.2877G>A (p.Thr959=)
NM_014780.5(CUL7):c.3257G>A (p.Gly1086Asp)
NM_014780.5(CUL7):c.3398G>A (p.Arg1133Gln)
NM_014780.5(CUL7):c.3645+34C>A
NM_014780.5(CUL7):c.4451_4452del (p.Val1484fs) rs730880261
NM_014780.5(CUL7):c.4617C>T (p.Asp1539=)
NM_014780.5(CUL7):c.4774-6C>T
NM_014780.5(CUL7):c.4917C>T (p.Asp1639=)
NM_014780.5(CUL7):c.711C>T (p.Phe237=)
NM_014780.5(CUL7):c.789C>A (p.Leu263=)
NM_014780.5(CUL7):c.816G>A (p.Ala272=)
NM_014780.5(CUL7):c.97G>A (p.Asp33Asn)

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