ClinVar Miner

List of variants in gene MEGF10 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 82
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001256545.2(MEGF10):c.1114C>T (p.Leu372=) rs31483 0.94572
NM_001256545.2(MEGF10):c.*209C>G rs10793809 0.74642
NM_001256545.2(MEGF10):c.*2236C>A rs3756722 0.73822
NM_001256545.2(MEGF10):c.-19+8919G>C rs1345662 0.53810
NM_001256545.2(MEGF10):c.3387T>A (p.Gly1129=) rs3812052 0.48209
NM_001256545.2(MEGF10):c.117-199A>G rs27782 0.39893
NM_001256545.2(MEGF10):c.-122G>A rs2032834 0.38334
NM_001256545.2(MEGF10):c.*2149G>A rs3756721 0.24708
NM_001256545.2(MEGF10):c.781-197A>C rs11952552 0.23313
NM_001256545.2(MEGF10):c.1130+141G>A rs3851469 0.22488
NM_001256545.2(MEGF10):c.2105-272A>C rs2408871 0.20278
NM_001256545.2(MEGF10):c.660-101A>G rs6595767 0.19743
NM_001256545.2(MEGF10):c.660-3C>T rs6595769 0.19743
NM_001256545.2(MEGF10):c.1785T>C (p.Pro595=) rs11950427 0.19610
NM_001256545.2(MEGF10):c.588G>A (p.Gln196=) rs3812055 0.16961
NM_001256545.2(MEGF10):c.3215G>A (p.Arg1072Lys) rs17164935 0.14236
NM_001256545.2(MEGF10):c.3026-252T>G rs72790443 0.13645
NM_001256545.2(MEGF10):c.2728+61T>C rs2270933 0.12698
NM_001256545.2(MEGF10):c.3233-58T>C rs3812053 0.10922
NM_001256545.2(MEGF10):c.616G>A (p.Val206Ile) rs3812054 0.10861
NM_001256545.2(MEGF10):c.659+302T>G rs72788599 0.10637
NM_001256545.2(MEGF10):c.2362+64T>G rs41298308 0.10584
NM_001256545.2(MEGF10):c.660-73C>T rs6595768 0.10504
NM_001256545.2(MEGF10):c.*625A>G rs72790451 0.10347
NM_001256545.2(MEGF10):c.3026-125A>T rs72790444 0.10326
NM_001256545.2(MEGF10):c.1975+43C>T rs72790419 0.10318
NM_001256545.2(MEGF10):c.2728+183G>A rs41298312 0.10041
NM_001256545.2(MEGF10):c.2234-124T>C rs60681812 0.09602
NM_001256545.2(MEGF10):c.1590+296G>C rs17673517 0.09463
NM_001256545.2(MEGF10):c.319+232A>G rs17165041 0.08751
NM_001256545.2(MEGF10):c.2856+181C>A rs58718502 0.07469
NM_001256545.2(MEGF10):c.*1246C>T rs17164925 0.07027
NM_001256545.2(MEGF10):c.2491+32C>T rs7737871 0.05291
NM_001256545.2(MEGF10):c.319+206T>C rs17839697 0.04973
NM_001256545.2(MEGF10):c.218+155G>A rs17673170 0.04936
NM_001256545.2(MEGF10):c.2105-322G>T rs73783795 0.04589
NM_001256545.2(MEGF10):c.3162G>A (p.Pro1054=) rs17164938 0.03315
NM_001256545.2(MEGF10):c.116+10T>C rs10519949 0.02763
NM_001256545.2(MEGF10):c.2199C>T (p.Cys733=) rs35591368 0.02614
NM_001256545.2(MEGF10):c.2076C>T (p.Pro692=) rs115309591 0.01810
NM_001256545.2(MEGF10):c.984C>T (p.Asn328=) rs35550094 0.01638
NM_001256545.2(MEGF10):c.3189G>A (p.Glu1063=) rs56157640 0.01628
NM_001256545.2(MEGF10):c.1841-20G>A rs79904777 0.01625
NM_001256545.2(MEGF10):c.218+188G>C rs57261222 0.01609
NM_001256545.2(MEGF10):c.-19+8943A>G rs79967765 0.00953
NM_001256545.2(MEGF10):c.609C>T (p.Cys203=) rs113794264 0.00845
NM_001256545.2(MEGF10):c.*4C>G rs73783802 0.00588
NM_001256545.2(MEGF10):c.1046G>A (p.Arg349His) rs78847357 0.00577
NM_001256545.2(MEGF10):c.489C>T (p.Ile163=) rs34649270 0.00577
NM_001256545.2(MEGF10):c.2757C>T (p.Asn919=) rs36061366 0.00492
NM_001256545.2(MEGF10):c.303C>T (p.Ser101=) rs77203884 0.00260
NM_001256545.2(MEGF10):c.218+17C>G rs72786483 0.00257
NM_001256545.2(MEGF10):c.1002C>T (p.His334=) rs142947482 0.00254
NM_001256545.2(MEGF10):c.1500G>A (p.Gln500=) rs146075981 0.00243
NM_001256545.2(MEGF10):c.2463C>T (p.Pro821=) rs139929890 0.00229
NM_001256545.2(MEGF10):c.2654G>A (p.Gly885Glu) rs116500162 0.00227
NM_001256545.2(MEGF10):c.3003C>T (p.Ser1001=) rs35159176 0.00207
NM_001256545.2(MEGF10):c.1564G>A (p.Gly522Arg) rs140563851 0.00178
NM_001256545.2(MEGF10):c.2034C>T (p.Asn678=) rs117124929 0.00145
NM_001256545.2(MEGF10):c.2857-8T>G rs201148765 0.00117
NM_001256545.2(MEGF10):c.1602C>T (p.Tyr534=) rs114704569 0.00116
NM_001256545.2(MEGF10):c.3026-8C>T rs185480820 0.00098
NM_001256545.2(MEGF10):c.117-5_117-4insC rs538399152 0.00081
NM_001256545.2(MEGF10):c.1975+10G>A rs148814585 0.00080
NM_001256545.2(MEGF10):c.2104+20A>C rs528070018 0.00034
NM_001256545.2(MEGF10):c.2175C>T (p.Ser725=) rs558369303 0.00006
NM_001256545.2(MEGF10):c.522G>A (p.Arg174=) rs201076330 0.00005
NM_001256545.2(MEGF10):c.1800C>T (p.Cys600=) rs528654275 0.00004
NM_001256545.2(MEGF10):c.3354C>G (p.Asp1118Glu) rs372767788 0.00003
NM_001256545.2(MEGF10):c.*3575T>G rs2898043
NM_001256545.2(MEGF10):c.-19+8702del rs35796097
NM_001256545.2(MEGF10):c.1131-280C>A rs79655685
NM_001256545.2(MEGF10):c.1306-278dup rs111958224
NM_001256545.2(MEGF10):c.174G>A (p.Thr58=) rs12654455
NM_001256545.2(MEGF10):c.1975+96_1975+118del rs11273003
NM_001256545.2(MEGF10):c.1976-7T>G
NM_001256545.2(MEGF10):c.2104+163del rs573923853
NM_001256545.2(MEGF10):c.219-333GA[3] rs147858479
NM_001256545.2(MEGF10):c.2857-292del rs199921206
NM_001256545.2(MEGF10):c.2857-292dup rs199921206
NM_001256545.2(MEGF10):c.3232+117TATTT[7] rs58939267
NM_001256545.2(MEGF10):c.412+226G>A rs1422318

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.