ClinVar Miner

List of variants in gene MEGF10 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 212
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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.-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.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.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.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.3026-272A>G rs115469299 0.03322
NM_001256545.2(MEGF10):c.3162G>A (p.Pro1054=) rs17164938 0.03315
NM_001256545.2(MEGF10):c.2981-165G>A rs41298322 0.03314
NM_001256545.2(MEGF10):c.3025+253A>G rs2270931 0.03312
NM_001256545.2(MEGF10):c.3233-299C>T rs17164929 0.03309
NM_001256545.2(MEGF10):c.3232+220C>G rs140094297 0.03297
NM_001256545.2(MEGF10):c.116+10T>C rs10519949 0.02763
NM_001256545.2(MEGF10):c.116+152G>A rs17684438 0.02654
NM_001256545.2(MEGF10):c.2199C>T (p.Cys733=) rs35591368 0.02614
NM_001256545.2(MEGF10):c.3233-176A>G rs17673727 0.02284
NM_001256545.2(MEGF10):c.1693+181G>A rs118151260 0.02169
NM_001256545.2(MEGF10):c.780+224C>T rs75840083 0.01815
NM_001256545.2(MEGF10):c.2076C>T (p.Pro692=) rs115309591 0.01810
NM_001256545.2(MEGF10):c.2105-103C>T rs76148405 0.01704
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.918-80C>G rs80313631 0.01603
NM_001256545.2(MEGF10):c.918-148T>C rs77896531 0.01602
NM_001256545.2(MEGF10):c.1305+238_1305+239del rs3051621 0.01600
NM_001256545.2(MEGF10):c.-18-179A>G rs80220399 0.01434
NM_001256545.2(MEGF10):c.1590+262T>A rs74823398 0.01298
NM_001256545.2(MEGF10):c.1841-283T>C rs41298306 0.01223
NM_001256545.2(MEGF10):c.3232+40T>C rs116650470 0.01118
NM_001256545.2(MEGF10):c.780+240G>A rs75289329 0.01036
NM_001256545.2(MEGF10):c.413-328C>G rs116710294 0.01007
NM_001256545.2(MEGF10):c.219-30G>A rs79602606 0.00957
NM_001256545.2(MEGF10):c.-19+8943A>G rs79967765 0.00953
NM_001256545.2(MEGF10):c.2981-272A>G rs76912327 0.00939
NM_001256545.2(MEGF10):c.659+265A>G rs116312116 0.00886
NM_001256545.2(MEGF10):c.609C>T (p.Cys203=) rs113794264 0.00845
NM_001256545.2(MEGF10):c.1975+260C>A rs141760181 0.00690
NM_001256545.2(MEGF10):c.412+135G>T rs143301955 0.00602
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.1426+124G>A rs141134404 0.00570
NM_001256545.2(MEGF10):c.1591-89A>G rs73783791 0.00566
NM_001256545.2(MEGF10):c.117-172C>T rs79417344 0.00558
NM_001256545.2(MEGF10):c.413-267A>G rs76602283 0.00558
NM_001256545.2(MEGF10):c.1305+111C>G rs186226957 0.00553
NM_001256545.2(MEGF10):c.1130+206A>G rs75203304 0.00544
NM_001256545.2(MEGF10):c.1427-197T>A rs6889554 0.00509
NM_001256545.2(MEGF10):c.2757C>T (p.Asn919=) rs36061366 0.00492
NM_001256545.2(MEGF10):c.1590+114G>A rs150014181 0.00474
NM_001256545.2(MEGF10):c.2491+210T>A rs193147523 0.00427
NM_001256545.2(MEGF10):c.1975+60C>T rs139297404 0.00361
NM_001256545.2(MEGF10):c.659+153A>C rs150309123 0.00353
NM_001256545.2(MEGF10):c.2105-80T>C rs115371829 0.00349
NM_001256545.2(MEGF10):c.1694-278C>G rs115627422 0.00320
NM_001256545.2(MEGF10):c.2857-329A>G rs192760223 0.00308
NM_001256545.2(MEGF10):c.660-244T>C rs112696032 0.00304
NM_001256545.2(MEGF10):c.2491+303A>G rs185245474 0.00300
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.-18-11C>T rs138523651 0.00240
NM_001256545.2(MEGF10):c.*52G>T rs182533165 0.00235
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.1626C>T (p.Cys542=) rs146902993 0.00129
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.3232+76T>C rs190980227 0.00116
NM_001256545.2(MEGF10):c.218+42G>A rs145752128 0.00098
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.1130+3G>A rs115184652 0.00076
NM_001256545.2(MEGF10):c.-19+8927A>T rs573144174 0.00054
NM_001256545.2(MEGF10):c.259A>G (p.Met87Val) rs41298304 0.00052
NM_001256545.2(MEGF10):c.1533C>T (p.Asp511=) rs151266058 0.00046
NM_001256545.2(MEGF10):c.452G>A (p.Arg151Gln) rs78069165 0.00039
NM_001256545.2(MEGF10):c.1622G>T (p.Arg541Leu) rs142664089 0.00035
NM_001256545.2(MEGF10):c.1130+12C>T rs201836299 0.00032
NM_001256545.2(MEGF10):c.50G>A (p.Cys17Tyr) rs145733370 0.00023
NM_001256545.2(MEGF10):c.877A>G (p.Thr293Ala) rs144187055 0.00022
NM_001256545.2(MEGF10):c.807C>T (p.Pro269=) rs146742773 0.00019
NM_001256545.2(MEGF10):c.2980+16G>A rs374003413 0.00017
NM_001256545.2(MEGF10):c.3170G>A (p.Arg1057Lys) rs374156507 0.00015
NM_001256545.2(MEGF10):c.401A>G (p.Asn134Ser) rs574376262 0.00013
NM_001256545.2(MEGF10):c.1839G>A (p.Arg613=) rs199930517 0.00011
NM_001256545.2(MEGF10):c.1130+13T>C rs746019129 0.00009
NM_001256545.2(MEGF10):c.1726C>T (p.Arg576Cys) rs143087353 0.00009
NM_001256545.2(MEGF10):c.2157T>C (p.His719=) rs374544972 0.00009
NM_001256545.2(MEGF10):c.2442T>C (p.Thr814=) rs370850456 0.00009
NM_001256545.2(MEGF10):c.2568C>T (p.Ile856=) rs778716392 0.00009
NM_001256545.2(MEGF10):c.2943G>A (p.Pro981=) rs371253627 0.00009
NM_001256545.2(MEGF10):c.120C>T (p.Tyr40=) rs372038844 0.00006
NM_001256545.2(MEGF10):c.1840+9C>G rs371418375 0.00006
NM_001256545.2(MEGF10):c.1959C>T (p.Gly653=) rs146017981 0.00006
NM_001256545.2(MEGF10):c.2104+7C>A rs371274853 0.00006
NM_001256545.2(MEGF10):c.2857-2A>G rs199750143 0.00006
NM_001256545.2(MEGF10):c.451C>T (p.Arg151Trp) rs767672691 0.00006
NM_001256545.2(MEGF10):c.2330G>A (p.Arg777His) rs565304206 0.00005
NM_001256545.2(MEGF10):c.3180A>G (p.Pro1060=) rs144450528 0.00005
NM_001256545.2(MEGF10):c.522G>A (p.Arg174=) rs201076330 0.00005
NM_001256545.2(MEGF10):c.917G>A (p.Arg306Gln) rs986353158 0.00005
NM_001256545.2(MEGF10):c.2590A>G (p.Ile864Val) rs780877446 0.00004
NM_001256545.2(MEGF10):c.2942C>T (p.Pro981Leu) rs1064793648 0.00004
NM_001256545.2(MEGF10):c.3033A>T (p.Gly1011=) rs745591064 0.00004
NM_001256545.2(MEGF10):c.-7G>A rs4620069 0.00003
NM_001256545.2(MEGF10):c.212G>A (p.Arg71Gln) rs886059862 0.00003
NM_001256545.2(MEGF10):c.2150A>G (p.Asn717Ser) rs116135607 0.00003
NM_001256545.2(MEGF10):c.2864A>C (p.Asn955Thr) rs1353393054 0.00003
NM_001256545.2(MEGF10):c.2320T>C (p.Cys774Arg) rs387907072 0.00002
NM_001256545.2(MEGF10):c.917+6G>T rs746095070 0.00002
NM_001256545.2(MEGF10):c.952G>A (p.Val318Ile) rs959864264 0.00002
NM_001256545.2(MEGF10):c.-19+8977C>T rs559140741 0.00001
NM_001256545.2(MEGF10):c.1008C>T (p.Ser336=) rs145815113 0.00001
NM_001256545.2(MEGF10):c.116+12G>C rs775584154 0.00001
NM_001256545.2(MEGF10):c.1278A>G (p.Gly426=) rs139438683 0.00001
NM_001256545.2(MEGF10):c.1322C>T (p.Thr441Ile) rs1160030961 0.00001
NM_001256545.2(MEGF10):c.1523A>G (p.Asn508Ser) rs184606767 0.00001
NM_001256545.2(MEGF10):c.1801G>A (p.Glu601Lys) rs778255998 0.00001
NM_001256545.2(MEGF10):c.1819C>T (p.Arg607Ter) rs1454219963 0.00001
NM_001256545.2(MEGF10):c.2362+2dup rs762560221 0.00001
NM_001256545.2(MEGF10):c.2576T>C (p.Ile859Thr) rs895294556 0.00001
NM_001256545.2(MEGF10):c.2853G>A (p.Thr951=) rs966689979 0.00001
NM_001256545.2(MEGF10):c.2980+9T>C rs779077674 0.00001
NM_001256545.2(MEGF10):c.3055A>G (p.Ser1019Gly) rs1766320871 0.00001
NM_001256545.2(MEGF10):c.3166C>T (p.Arg1056Ter) rs989552169 0.00001
NM_001256545.2(MEGF10):c.3278G>A (p.Arg1093His) rs187800437 0.00001
NM_001256545.2(MEGF10):c.529C>T (p.Arg177Cys) rs748641801 0.00001
NM_001256545.2(MEGF10):c.59T>C (p.Ile20Thr) rs748919606 0.00001
NM_001256545.2(MEGF10):c.930G>A (p.Glu310=) rs1264341592 0.00001
NM_001256545.2(MEGF10):c.935C>T (p.Pro312Leu) rs199702225 0.00001
NM_001256545.2(MEGF10):c.-18-12dup rs774762160
NM_001256545.2(MEGF10):c.-19+8702del rs35796097
NM_001256545.2(MEGF10):c.-19+8933A>G rs1057522065
NM_001256545.2(MEGF10):c.1075C>T (p.Leu359Phe) rs754958105
NM_001256545.2(MEGF10):c.1099C>T (p.Arg367Trp)
NM_001256545.2(MEGF10):c.1131-280C>A rs79655685
NM_001256545.2(MEGF10):c.1192G>T (p.Glu398Ter) rs200174116
NM_001256545.2(MEGF10):c.1292C>T (p.Ala431Val) rs1057518319
NM_001256545.2(MEGF10):c.1306-278dup rs111958224
NM_001256545.2(MEGF10):c.1643A>T (p.Asp548Val) rs1338867391
NM_001256545.2(MEGF10):c.1673G>T (p.Arg558Leu) rs182243856
NM_001256545.2(MEGF10):c.174G>A (p.Thr58=) rs12654455
NM_001256545.2(MEGF10):c.174G>T (p.Thr58=) rs12654455
NM_001256545.2(MEGF10):c.1975+96_1975+118del rs11273003
NM_001256545.2(MEGF10):c.2104+163del rs573923853
NM_001256545.2(MEGF10):c.2104+252C>T rs147085199
NM_001256545.2(MEGF10):c.2144C>A (p.Thr715Lys) rs147731088
NM_001256545.2(MEGF10):c.217dup (p.Arg73fs) rs1291487750
NM_001256545.2(MEGF10):c.219-333GA[3] rs147858479
NM_001256545.2(MEGF10):c.2301C>A (p.Cys767Ter) rs387907071
NM_001256545.2(MEGF10):c.2363A>G (p.Lys788Arg) rs1200074021
NM_001256545.2(MEGF10):c.2407del (p.Asp803fs) rs1064795948
NM_001256545.2(MEGF10):c.2411G>A (p.Cys804Tyr) rs1057523896
NM_001256545.2(MEGF10):c.2729-279C>A rs2003863
NM_001256545.2(MEGF10):c.2729-279C>T rs2003863
NM_001256545.2(MEGF10):c.2742C>A (p.His914Gln) rs2127029173
NM_001256545.2(MEGF10):c.2743A>C (p.Ser915Arg) rs1387603431
NM_001256545.2(MEGF10):c.2785A>T (p.Ser929Cys) rs1561653221
NM_001256545.2(MEGF10):c.2819C>T (p.Pro940Leu) rs1765999410
NM_001256545.2(MEGF10):c.2857-292del rs199921206
NM_001256545.2(MEGF10):c.2857-292dup rs199921206
NM_001256545.2(MEGF10):c.2980+249G>C rs41298316
NM_001256545.2(MEGF10):c.3026-273_3026-269del rs200590009
NM_001256545.2(MEGF10):c.3123G>A (p.Pro1041=) rs764182965
NM_001256545.2(MEGF10):c.320-134_320-130del rs141639621
NM_001256545.2(MEGF10):c.3215_3216delinsAC (p.Arg1072Asn) rs386692223
NM_001256545.2(MEGF10):c.3232+117TATTT[7] rs58939267
NM_001256545.2(MEGF10):c.3272A>G (p.Asn1091Ser)
NM_001256545.2(MEGF10):c.3331T>C (p.Tyr1111His) rs1064795277
NM_001256545.2(MEGF10):c.3415_3417dup (p.Ser1139dup) rs2127049632
NM_001256545.2(MEGF10):c.412+127C>G rs115315224
NM_001256545.2(MEGF10):c.412+226G>A rs1422318
NM_001256545.2(MEGF10):c.625G>T (p.Glu209Ter) rs1064793831
NM_001256545.2(MEGF10):c.733G>T (p.Val245Leu) rs755790851
NM_001256545.2(MEGF10):c.786A>G (p.Thr262=) rs893078096
NM_001256545.2(MEGF10):c.789G>T (p.Val263=) rs1188804374
NM_001256545.2(MEGF10):c.917+230dup rs112880381
NM_001256545.2(MEGF10):c.918-141G>C rs76221063

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