ClinVar Miner

List of variants in gene MEGF8 reported as likely benign for acrocephalopolysyndactyly

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 214
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HGVS dbSNP gnomAD frequency
NM_001271938.2(MEGF8):c.7673C>T (p.Pro2558Leu) rs147216997 0.00639
NM_001271938.2(MEGF8):c.7421G>A (p.Arg2474His) rs45623135 0.00308
NM_001271938.2(MEGF8):c.6481+11T>G rs138919410 0.00270
NM_001271938.2(MEGF8):c.7705G>A (p.Val2569Ile) rs147133204 0.00251
NM_001271938.2(MEGF8):c.8176C>T (p.Arg2726Cys) rs141224456 0.00186
NM_001271938.2(MEGF8):c.5344-14C>T rs369531263 0.00097
NM_001271938.2(MEGF8):c.2454C>T (p.Ser818=) rs140035679 0.00096
NM_001271938.2(MEGF8):c.7136+10A>C rs750945705 0.00096
NM_001271938.2(MEGF8):c.3455C>T (p.Pro1152Leu) rs367649187 0.00091
NM_001271938.2(MEGF8):c.7567A>G (p.Thr2523Ala) rs139192223 0.00074
NM_001271938.2(MEGF8):c.8433C>T (p.His2811=) rs371191311 0.00067
NM_001271938.2(MEGF8):c.3033C>T (p.Thr1011=) rs145216125 0.00061
NM_001271938.2(MEGF8):c.3154T>C (p.Trp1052Arg) rs202039332 0.00060
NM_001271938.2(MEGF8):c.3843G>A (p.Arg1281=) rs148792547 0.00058
NM_001271938.2(MEGF8):c.281C>T (p.Pro94Leu) rs570125469 0.00045
NM_001271938.2(MEGF8):c.6274-9C>G rs373417416 0.00041
NM_001271938.2(MEGF8):c.7089C>T (p.Cys2363=) rs138235390 0.00037
NM_001271938.2(MEGF8):c.390G>A (p.Leu130=) rs377093238 0.00034
NM_001271938.2(MEGF8):c.5512A>G (p.Met1838Val) rs200501111 0.00031
NM_001271938.2(MEGF8):c.8271C>T (p.Pro2757=) rs755400663 0.00031
NM_001271938.2(MEGF8):c.6395G>A (p.Arg2132Gln) rs201140958 0.00027
NM_001271938.2(MEGF8):c.3873G>A (p.Gly1291=) rs373710119 0.00026
NM_001271938.2(MEGF8):c.4041C>T (p.Phe1347=) rs148895205 0.00026
NM_001271938.2(MEGF8):c.1275T>C (p.Leu425=) rs370779185 0.00025
NM_001271938.2(MEGF8):c.3625C>T (p.Arg1209Trp) rs372257661 0.00025
NM_001271938.2(MEGF8):c.8373C>T (p.Pro2791=) rs374532854 0.00023
NM_001271938.2(MEGF8):c.8133G>A (p.Pro2711=) rs370578585 0.00022
NM_001271938.2(MEGF8):c.740-6C>T rs372546741 0.00020
NM_001271938.2(MEGF8):c.5492C>T (p.Ser1831Leu) rs139959427 0.00019
NM_001271938.2(MEGF8):c.5937G>A (p.Arg1979=) rs200310970 0.00017
NM_001271938.2(MEGF8):c.5559G>A (p.Leu1853=) rs36016565 0.00016
NM_001271938.2(MEGF8):c.2987+11del rs755747202 0.00015
NM_001271938.2(MEGF8):c.4434C>T (p.Pro1478=) rs371090576 0.00015
NM_001271938.2(MEGF8):c.2537C>T (p.Ser846Leu) rs148207079 0.00014
NM_001271938.2(MEGF8):c.4752G>C (p.Leu1584=) rs541175277 0.00014
NM_001271938.2(MEGF8):c.5343+9T>G rs374168560 0.00014
NM_001271938.2(MEGF8):c.1933+10C>T rs763206386 0.00013
NM_001271938.2(MEGF8):c.3310C>T (p.Arg1104Trp) rs370522595 0.00013
NM_001271938.2(MEGF8):c.351+10G>A rs374212597 0.00013
NM_001271938.2(MEGF8):c.7047C>T (p.Ala2349=) rs369359832 0.00012
NM_001271938.2(MEGF8):c.3798C>T (p.Arg1266=) rs750232469 0.00011
NM_001271938.2(MEGF8):c.4662G>A (p.Ala1554=) rs759312023 0.00011
NM_001271938.2(MEGF8):c.6469G>A (p.Gly2157Ser) rs549617171 0.00010
NM_001271938.2(MEGF8):c.2436G>A (p.Ser812=) rs199938628 0.00009
NM_001271938.2(MEGF8):c.2649T>C (p.Asp883=) rs757551016 0.00009
NM_001271938.2(MEGF8):c.7407G>A (p.Ala2469=) rs111595088 0.00009
NM_001271938.2(MEGF8):c.8169C>T (p.Pro2723=) rs138179740 0.00009
NM_001271938.2(MEGF8):c.3456G>A (p.Pro1152=) rs200838638 0.00008
NM_001271938.2(MEGF8):c.6909C>T (p.His2303=) rs552181649 0.00008
NM_001271938.2(MEGF8):c.2856-4C>G rs749739307 0.00007
NM_001271938.2(MEGF8):c.3761+19C>A rs371147358 0.00007
NM_001271938.2(MEGF8):c.3846C>T (p.Val1282=) rs142473307 0.00007
NM_001271938.2(MEGF8):c.5382G>A (p.Gly1794=) rs905021679 0.00007
NM_001271938.2(MEGF8):c.6426G>A (p.Gly2142=) rs772127120 0.00007
NM_001271938.2(MEGF8):c.1789-5C>T rs752609842 0.00006
NM_001271938.2(MEGF8):c.2784G>A (p.Ala928=) rs750686408 0.00006
NM_001271938.2(MEGF8):c.3951C>T (p.Pro1317=) rs139891048 0.00006
NM_001271938.2(MEGF8):c.6753G>A (p.Thr2251=) rs372437317 0.00006
NM_001271938.2(MEGF8):c.7311C>T (p.Gly2437=) rs375011847 0.00006
NM_001271938.2(MEGF8):c.7713G>A (p.Pro2571=) rs200748447 0.00006
NM_001271938.2(MEGF8):c.352-5C>T rs180788941 0.00005
NM_001271938.2(MEGF8):c.3350+11C>T rs201865376 0.00004
NM_001271938.2(MEGF8):c.3957C>A (p.Thr1319=) rs754753739 0.00004
NM_001271938.2(MEGF8):c.3990C>T (p.Pro1330=) rs141015952 0.00004
NM_001271938.2(MEGF8):c.4416C>T (p.Ala1472=) rs139822806 0.00004
NM_001271938.2(MEGF8):c.6059-18C>A rs565505835 0.00004
NM_001271938.2(MEGF8):c.6274-8C>G rs543093080 0.00004
NM_001271938.2(MEGF8):c.6588C>T (p.His2196=) rs751105144 0.00004
NM_001271938.2(MEGF8):c.7893C>T (p.Ala2631=) rs150486662 0.00004
NM_001271938.2(MEGF8):c.1707C>T (p.Ser569=) rs201780276 0.00003
NM_001271938.2(MEGF8):c.2961C>T (p.His987=) rs760802467 0.00003
NM_001271938.2(MEGF8):c.3648C>T (p.His1216=) rs144358189 0.00003
NM_001271938.2(MEGF8):c.5556C>T (p.Arg1852=) rs756300122 0.00003
NM_001271938.2(MEGF8):c.5601G>C (p.Leu1867=) rs772768540 0.00003
NM_001271938.2(MEGF8):c.5907T>C (p.Asn1969=) rs751281117 0.00003
NM_001271938.2(MEGF8):c.6093C>T (p.Thr2031=) rs992577271 0.00003
NM_001271938.2(MEGF8):c.6705C>T (p.Pro2235=) rs149735243 0.00003
NM_001271938.2(MEGF8):c.2724C>T (p.His908=) rs752713774 0.00002
NM_001271938.2(MEGF8):c.5364C>T (p.His1788=) rs1038902556 0.00002
NM_001271938.2(MEGF8):c.6540C>T (p.Asp2180=) rs781099770 0.00002
NM_001271938.2(MEGF8):c.6834+11C>T rs369152755 0.00002
NM_001271938.2(MEGF8):c.7099C>T (p.Leu2367=) rs768745459 0.00002
NM_001271938.2(MEGF8):c.7184C>T (p.Thr2395Met) rs758007485 0.00002
NM_001271938.2(MEGF8):c.123A>G (p.Pro41=) rs964840099 0.00001
NM_001271938.2(MEGF8):c.1791T>C (p.Cys597=) rs777831498 0.00001
NM_001271938.2(MEGF8):c.3378G>A (p.Val1126=) rs780556649 0.00001
NM_001271938.2(MEGF8):c.3804C>T (p.Leu1268=) rs780442723 0.00001
NM_001271938.2(MEGF8):c.5583A>C (p.Gly1861=) rs746270596 0.00001
NM_001271938.2(MEGF8):c.5853C>A (p.Thr1951=) rs754567747 0.00001
NM_001271938.2(MEGF8):c.6059-16C>T rs760323076 0.00001
NM_001271938.2(MEGF8):c.610C>T (p.Leu204=) rs1351465017 0.00001
NM_001271938.2(MEGF8):c.6261C>T (p.Ser2087=) rs2039558834 0.00001
NM_001271938.2(MEGF8):c.6482-9C>T rs776227273 0.00001
NM_001271938.2(MEGF8):c.6693A>C (p.Ser2231=) rs746097325 0.00001
NM_001271938.2(MEGF8):c.6936C>A (p.Ile2312=) rs764031754 0.00001
NM_001271938.2(MEGF8):c.6966C>T (p.Ser2322=) rs754666704 0.00001
NM_001271938.2(MEGF8):c.7155C>T (p.His2385=) rs775919574 0.00001
NM_001271938.2(MEGF8):c.7368G>A (p.Thr2456=) rs779163527 0.00001
NM_001271938.2(MEGF8):c.948C>A (p.Gly316=) rs971549656 0.00001
NM_001271938.2(MEGF8):c.1005A>G (p.Ala335=) rs2039124115
NM_001271938.2(MEGF8):c.1014G>A (p.Ala338=)
NM_001271938.2(MEGF8):c.1137G>C (p.Val379=) rs1219090266
NM_001271938.2(MEGF8):c.1245-11T>G
NM_001271938.2(MEGF8):c.1497G>A (p.Pro499=)
NM_001271938.2(MEGF8):c.1557G>A (p.Ala519=)
NM_001271938.2(MEGF8):c.1669-8C>T
NM_001271938.2(MEGF8):c.1797C>T (p.Ala599=) rs749153853
NM_001271938.2(MEGF8):c.1934-12C>G rs2147465024
NM_001271938.2(MEGF8):c.1934-21_1934-18del rs2039263296
NM_001271938.2(MEGF8):c.2073G>A (p.Pro691=)
NM_001271938.2(MEGF8):c.2340G>A (p.Thr780=) rs776196677
NM_001271938.2(MEGF8):c.2355C>A (p.Arg785=)
NM_001271938.2(MEGF8):c.246G>T (p.Thr82=) rs369259465
NM_001271938.2(MEGF8):c.2500-10C>T
NM_001271938.2(MEGF8):c.261C>T (p.Phe87=)
NM_001271938.2(MEGF8):c.2643C>T (p.Cys881=)
NM_001271938.2(MEGF8):c.2751G>A (p.Glu917=)
NM_001271938.2(MEGF8):c.2796G>T (p.Arg932=)
NM_001271938.2(MEGF8):c.282G>C (p.Pro94=)
NM_001271938.2(MEGF8):c.2855+12T>C
NM_001271938.2(MEGF8):c.291G>T (p.Pro97=)
NM_001271938.2(MEGF8):c.2982C>T (p.Asp994=)
NM_001271938.2(MEGF8):c.3057C>T (p.His1019=)
NM_001271938.2(MEGF8):c.3228T>C (p.Asp1076=)
NM_001271938.2(MEGF8):c.3294C>T (p.Tyr1098=)
NM_001271938.2(MEGF8):c.3350+12G>A
NM_001271938.2(MEGF8):c.3351-11C>T
NM_001271938.2(MEGF8):c.3426A>G (p.Thr1142=)
NM_001271938.2(MEGF8):c.3498C>T (p.Ser1166=) rs1600051149
NM_001271938.2(MEGF8):c.351+18C>T
NM_001271938.2(MEGF8):c.351+20T>C
NM_001271938.2(MEGF8):c.352-16C>T
NM_001271938.2(MEGF8):c.3588C>T (p.Pro1196=)
NM_001271938.2(MEGF8):c.4012-4C>G rs1405166507
NM_001271938.2(MEGF8):c.4074G>A (p.Ser1358=)
NM_001271938.2(MEGF8):c.4149G>A (p.Leu1383=)
NM_001271938.2(MEGF8):c.4200T>C (p.Ala1400=)
NM_001271938.2(MEGF8):c.4212T>G (p.Ser1404=)
NM_001271938.2(MEGF8):c.4251C>T (p.Val1417=)
NM_001271938.2(MEGF8):c.4275C>T (p.Asp1425=)
NM_001271938.2(MEGF8):c.428C>A (p.Pro143Gln)
NM_001271938.2(MEGF8):c.4365C>T (p.Ala1455=)
NM_001271938.2(MEGF8):c.4393-19G>C
NM_001271938.2(MEGF8):c.4407C>T (p.Cys1469=)
NM_001271938.2(MEGF8):c.4504-11C>T
NM_001271938.2(MEGF8):c.4567T>C (p.Leu1523=) rs2039453501
NM_001271938.2(MEGF8):c.4623-5C>A
NM_001271938.2(MEGF8):c.4668C>T (p.Ala1556=)
NM_001271938.2(MEGF8):c.4764C>T (p.Thr1588=)
NM_001271938.2(MEGF8):c.4831-11C>T
NM_001271938.2(MEGF8):c.4968C>T (p.Thr1656=)
NM_001271938.2(MEGF8):c.4989C>A (p.Ala1663=)
NM_001271938.2(MEGF8):c.5007C>A (p.Pro1669=) rs755932452
NM_001271938.2(MEGF8):c.5025C>T (p.His1675=) rs2147488751
NM_001271938.2(MEGF8):c.5049C>T (p.Thr1683=)
NM_001271938.2(MEGF8):c.5100C>A (p.Ala1700=)
NM_001271938.2(MEGF8):c.5176-12C>G
NM_001271938.2(MEGF8):c.5176-18C>T
NM_001271938.2(MEGF8):c.519G>A (p.Glu173=)
NM_001271938.2(MEGF8):c.5275A>G (p.Met1759Val)
NM_001271938.2(MEGF8):c.5281C>G (p.Leu1761Val) rs150607375
NM_001271938.2(MEGF8):c.5343+16G>A
NM_001271938.2(MEGF8):c.5343+17G>A rs2147490241
NM_001271938.2(MEGF8):c.5344-16C>A
NM_001271938.2(MEGF8):c.5344-17C>A rs780933404
NM_001271938.2(MEGF8):c.5376G>C (p.Leu1792=) rs2147490712
NM_001271938.2(MEGF8):c.5427C>T (p.Phe1809=)
NM_001271938.2(MEGF8):c.5478C>T (p.Pro1826=)
NM_001271938.2(MEGF8):c.5555G>A (p.Arg1852His)
NM_001271938.2(MEGF8):c.5577C>T (p.Phe1859=)
NM_001271938.2(MEGF8):c.559-18_559-17del rs2147448565
NM_001271938.2(MEGF8):c.559-5C>T
NM_001271938.2(MEGF8):c.5720+12G>A
NM_001271938.2(MEGF8):c.5720+19A>C rs2039524149
NM_001271938.2(MEGF8):c.5733G>A (p.Gly1911=)
NM_001271938.2(MEGF8):c.5847G>A (p.Ala1949=)
NM_001271938.2(MEGF8):c.6039G>A (p.Thr2013=)
NM_001271938.2(MEGF8):c.6058+5G>T
NM_001271938.2(MEGF8):c.6081C>T (p.Ser2027=)
NM_001271938.2(MEGF8):c.6087G>A (p.Gln2029=)
NM_001271938.2(MEGF8):c.6105G>A (p.Thr2035=)
NM_001271938.2(MEGF8):c.6163C>T (p.Leu2055=)
NM_001271938.2(MEGF8):c.6267G>A (p.Leu2089=) rs934116600
NM_001271938.2(MEGF8):c.6274-18C>T
NM_001271938.2(MEGF8):c.6274-7C>G
NM_001271938.2(MEGF8):c.6274-7C>T rs772512683
NM_001271938.2(MEGF8):c.6312C>T (p.Ala2104=)
NM_001271938.2(MEGF8):c.6381C>T (p.Cys2127=) rs532126083
NM_001271938.2(MEGF8):c.6474C>T (p.Pro2158=)
NM_001271938.2(MEGF8):c.648C>T (p.His216=)
NM_001271938.2(MEGF8):c.699C>T (p.Gly233=)
NM_001271938.2(MEGF8):c.7116C>G (p.Leu2372=)
NM_001271938.2(MEGF8):c.7248T>C (p.Arg2416=)
NM_001271938.2(MEGF8):c.7270-5C>T
NM_001271938.2(MEGF8):c.7296C>T (p.His2432=)
NM_001271938.2(MEGF8):c.735C>T (p.Phe245=)
NM_001271938.2(MEGF8):c.739+11G>C
NM_001271938.2(MEGF8):c.7422C>T (p.Arg2474=)
NM_001271938.2(MEGF8):c.7560C>T (p.Gly2520=)
NM_001271938.2(MEGF8):c.7590A>G (p.Pro2530=)
NM_001271938.2(MEGF8):c.7674G>C (p.Pro2558=) rs774279106
NM_001271938.2(MEGF8):c.771C>T (p.Leu257=)
NM_001271938.2(MEGF8):c.7743G>A (p.Thr2581=)
NM_001271938.2(MEGF8):c.7758G>A (p.Val2586=)
NM_001271938.2(MEGF8):c.7770C>T (p.Arg2590=)
NM_001271938.2(MEGF8):c.7854C>T (p.Gly2618=)
NM_001271938.2(MEGF8):c.7893C>G (p.Ala2631=) rs150486662
NM_001271938.2(MEGF8):c.7959C>T (p.Ser2653=)
NM_001271938.2(MEGF8):c.7968C>T (p.Phe2656=)
NM_001271938.2(MEGF8):c.8103C>T (p.Thr2701=)
NM_001271938.2(MEGF8):c.8109C>T (p.Cys2703=)
NM_001271938.2(MEGF8):c.8466_8467delinsAG (p.Ser2823Gly) rs2039775950
NM_001271938.2(MEGF8):c.8532C>T (p.Ser2844=)
NM_001271938.2(MEGF8):c.937C>T (p.Leu313=)

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