ClinVar Miner

List of variants in gene CUL7 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
Download table as spreadsheet
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.581-165G>A rs41274916 0.23752
NM_014780.5(CUL7):c.339C>T (p.Asp113=) rs4711738 0.22523
NM_014780.5(CUL7):c.2766+62A>G rs2273918 0.14189
NM_014780.5(CUL7):c.3646-63T>C rs11961678 0.11025
NM_014780.5(CUL7):c.2169+180C>T rs1079325 0.09515
NM_014780.5(CUL7):c.4295-257A>G rs3805945 0.08712
NM_014780.5(CUL7):c.2489-32C>T rs111320577 0.04049
NM_014780.5(CUL7):c.3173-271C>T rs58300975 0.02747
NM_014780.5(CUL7):c.4294+257G>A rs113218760 0.02712
NM_014780.5(CUL7):c.4794G>A (p.Lys1598=) rs61437700 0.02584
NM_014780.5(CUL7):c.3038+109G>A rs57516312 0.02519
NM_014780.5(CUL7):c.3172+211C>G rs114838794 0.02516
NM_014780.5(CUL7):c.2555G>A (p.Arg852Gln) rs34574340 0.02119
NM_014780.5(CUL7):c.2612C>T (p.Ala871Val) rs61732148 0.01767
NM_014780.5(CUL7):c.1202G>A (p.Arg401Gln) rs73733791 0.01429
NM_014780.5(CUL7):c.1027C>T (p.Pro343Ser) rs113845886 0.01387
NM_014780.5(CUL7):c.3096C>T (p.Asp1032=) rs138276478 0.01292
NM_014780.5(CUL7):c.1846A>G (p.Ser616Gly) rs7774330 0.01270
NM_014780.5(CUL7):c.4762C>A (p.Leu1588Ile) rs147493246 0.00727
NM_014780.5(CUL7):c.1780G>A (p.Ala594Thr) rs141065679 0.00707
NM_014780.5(CUL7):c.4463T>C (p.Leu1488Pro) rs41274912 0.00688
NM_014780.5(CUL7):c.5088C>T (p.Thr1696=) rs73733789 0.00426
NM_014780.5(CUL7):c.4914C>T (p.Asp1638=) rs61731584 0.00197
NM_014780.5(CUL7):c.861G>A (p.Gly287=) rs61750322 0.00140
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.3490C>T (p.Arg1164Trp) rs201135654 0.00102
NM_014780.5(CUL7):c.465A>T (p.Gly155=) rs150212051 0.00094
NM_014780.5(CUL7):c.2803C>T (p.Leu935=) rs146309619 0.00091
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.4323C>T (p.Gly1441=) rs148472550 0.00066
NM_014780.5(CUL7):c.4898C>T (p.Thr1633Met) rs139249497 0.00063
NM_014780.5(CUL7):c.4935C>T (p.Ser1645=) rs116910528 0.00049
NM_014780.5(CUL7):c.3876C>T (p.Ile1292=) rs147056081 0.00046
NM_014780.5(CUL7):c.1030G>A (p.Ala344Thr) rs183119565 0.00042
NM_014780.5(CUL7):c.4731C>T (p.Ala1577=) rs141716467 0.00038
NM_014780.5(CUL7):c.1542G>T (p.Gln514His) rs146808129 0.00036
NM_014780.5(CUL7):c.3432G>A (p.Thr1144=) rs144556973 0.00036
NM_014780.5(CUL7):c.2488+16C>T rs117068976 0.00034
NM_014780.5(CUL7):c.3416T>C (p.Ile1139Thr) rs77965460 0.00034
NM_014780.5(CUL7):c.4261A>G (p.Thr1421Ala) rs191578513 0.00024
NM_014780.5(CUL7):c.1716C>G (p.Ala572=) rs150213603 0.00023
NM_014780.5(CUL7):c.687G>A (p.Thr229=) rs192945321 0.00019
NM_014780.5(CUL7):c.2603A>G (p.Asn868Ser) rs149360738 0.00007
NM_014780.5(CUL7):c.4417C>T (p.Leu1473=) rs201386557 0.00004
NM_014780.5(CUL7):c.1823A>G (p.Glu608Gly) rs199819170 0.00002
NM_014780.5(CUL7):c.1215C>T (p.Asn405=) rs755095253 0.00001
NM_014780.5(CUL7):c.2307T>C (p.Ala769=) rs538588226 0.00001
NC_000006.12:g.43037427CT[3] rs34475602
NM_014780.5(CUL7):c.1168GAG[1] (p.Glu391del) rs372224208
NM_014780.5(CUL7):c.1234-207GT[18] rs58059598
NM_014780.5(CUL7):c.1234-207GT[19] rs58059598
NM_014780.5(CUL7):c.1234-207GT[20] rs58059598
NM_014780.5(CUL7):c.1234-207GT[25] rs58059598
NM_014780.5(CUL7):c.1234-207GT[26] rs58059598
NM_014780.5(CUL7):c.1234-207GT[27] rs58059598
NM_014780.5(CUL7):c.2229C>G (p.Ala743=) rs188565648
NM_014780.5(CUL7):c.2438_2439delinsGG (p.Gln813Arg) rs61748654
NM_014780.5(CUL7):c.2767-7dup
NM_014780.5(CUL7):c.3172+254del rs35607536
NM_014780.5(CUL7):c.4295-14C>A rs144154816
NM_014780.5(CUL7):c.4295-174C>A rs58659748
NM_014780.5(CUL7):c.732+14del rs765319655

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.