ClinVar Miner

List of variants in gene MEGF8 reported as uncertain significance for not provided

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Gene type:
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Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_001271938.2(MEGF8):c.8176C>T (p.Arg2726Cys) rs141224456 0.00186
NM_001271938.2(MEGF8):c.7774G>A (p.Val2592Met) rs148860986 0.00105
NM_001271938.2(MEGF8):c.3455C>T (p.Pro1152Leu) rs367649187 0.00091
NM_001271938.2(MEGF8):c.3010C>T (p.Arg1004Trp) rs141383715 0.00084
NM_001271938.2(MEGF8):c.2357C>G (p.Pro786Arg) rs114954140 0.00068
NM_001271938.2(MEGF8):c.3154T>C (p.Trp1052Arg) rs202039332 0.00060
NM_001271938.2(MEGF8):c.7048G>A (p.Val2350Met) rs73033442 0.00055
NM_001271938.2(MEGF8):c.2450A>G (p.His817Arg) rs151116615 0.00039
NM_001271938.2(MEGF8):c.1024G>A (p.Val342Met) rs372990477 0.00029
NM_001271938.2(MEGF8):c.5018A>G (p.Tyr1673Cys) rs143215498 0.00029
NM_001271938.2(MEGF8):c.6395G>A (p.Arg2132Gln) rs201140958 0.00027
NM_001271938.2(MEGF8):c.3626G>A (p.Arg1209Gln) rs556378666 0.00024
NM_001271938.2(MEGF8):c.4675G>A (p.Gly1559Arg) rs760852092 0.00008
NM_001271938.2(MEGF8):c.5353C>T (p.Arg1785Trp) rs772299336 0.00006
NM_001271938.2(MEGF8):c.5740C>G (p.Pro1914Ala) rs147084460 0.00006
NM_001271938.2(MEGF8):c.6500C>T (p.Pro2167Leu) rs372350131 0.00006
NM_001271938.2(MEGF8):c.3841C>T (p.Arg1281Trp) rs371283114 0.00005
NM_001271938.2(MEGF8):c.4516C>T (p.Arg1506Cys) rs142361779 0.00005
NM_001271938.2(MEGF8):c.8492G>A (p.Arg2831Gln) rs766621187 0.00005
NM_001271938.2(MEGF8):c.485C>T (p.Pro162Leu) rs770734416 0.00004
NM_001271938.2(MEGF8):c.8284G>A (p.Gly2762Arg) rs770472361 0.00004
NM_001271938.2(MEGF8):c.1057C>T (p.Arg353Cys) rs554274233 0.00003
NM_001271938.2(MEGF8):c.3392C>T (p.Pro1131Leu) rs748525586 0.00003
NM_001271938.2(MEGF8):c.4289C>T (p.Ala1430Val) rs777183202 0.00003
NM_001271938.2(MEGF8):c.5411C>T (p.Ser1804Leu) rs757227265 0.00003
NM_001271938.2(MEGF8):c.5581G>A (p.Gly1861Arg) rs774973725 0.00003
NM_001271938.2(MEGF8):c.1079C>T (p.Ser360Phe) rs1064796651 0.00002
NM_001271938.2(MEGF8):c.1315C>T (p.Arg439Trp) rs769862975 0.00002
NM_001271938.2(MEGF8):c.2485G>A (p.Val829Met) rs530378456 0.00002
NM_001271938.2(MEGF8):c.412C>T (p.Arg138Cys) rs760894078 0.00002
NM_001271938.2(MEGF8):c.4492C>T (p.Arg1498Cys) rs747096596 0.00002
NM_001271938.2(MEGF8):c.4661C>T (p.Ala1554Val) rs774083503 0.00002
NM_001271938.2(MEGF8):c.2173T>A (p.Phe725Ile) rs1050470092 0.00001
NM_001271938.2(MEGF8):c.2477G>A (p.Arg826Gln) rs775071124 0.00001
NM_001271938.2(MEGF8):c.3037C>G (p.His1013Asp) rs761975438 0.00001
NM_001271938.2(MEGF8):c.4237G>A (p.Gly1413Arg) rs768127043 0.00001
NM_001271938.2(MEGF8):c.4363G>A (p.Ala1455Thr) rs2039445965 0.00001
NM_001271938.2(MEGF8):c.4655T>C (p.Met1552Thr) rs901194855 0.00001
NM_001271938.2(MEGF8):c.5407C>T (p.Arg1803Cys) rs755807533 0.00001
NM_001271938.2(MEGF8):c.5422G>A (p.Glu1808Lys) rs771890594 0.00001
NM_001271938.2(MEGF8):c.6295C>T (p.Pro2099Ser) rs1471300485 0.00001
NM_001271938.2(MEGF8):c.6310G>T (p.Ala2104Ser) rs772768716 0.00001
NM_001271938.2(MEGF8):c.6440G>A (p.Gly2147Asp) rs763943694 0.00001
NM_001271938.2(MEGF8):c.901G>A (p.Gly301Ser) rs369528104 0.00001
NM_001271938.2(MEGF8):c.1031A>G (p.Asp344Gly)
NM_001271938.2(MEGF8):c.1312G>T (p.Gly438Trp)
NM_001271938.2(MEGF8):c.2230G>A (p.Val744Met)
NM_001271938.2(MEGF8):c.2269A>G (p.Met757Val)
NM_001271938.2(MEGF8):c.2530C>G (p.Arg844Gly)
NM_001271938.2(MEGF8):c.2624G>A (p.Arg875His)
NM_001271938.2(MEGF8):c.2635G>T (p.Ala879Ser)
NM_001271938.2(MEGF8):c.2866T>C (p.Cys956Arg)
NM_001271938.2(MEGF8):c.3133G>A (p.Gly1045Ser) rs756780589
NM_001271938.2(MEGF8):c.3223G>A (p.Val1075Met)
NM_001271938.2(MEGF8):c.3643G>A (p.Gly1215Arg)
NM_001271938.2(MEGF8):c.3782G>A (p.Arg1261Gln)
NM_001271938.2(MEGF8):c.3931G>A (p.Glu1311Lys)
NM_001271938.2(MEGF8):c.4430G>T (p.Gly1477Val)
NM_001271938.2(MEGF8):c.4435G>A (p.Asp1479Asn)
NM_001271938.2(MEGF8):c.4835C>A (p.Pro1612His) rs138397020
NM_001271938.2(MEGF8):c.497G>T (p.Gly166Val)
NM_001271938.2(MEGF8):c.6021G>C (p.Glu2007Asp) rs1235208244
NM_001271938.2(MEGF8):c.6307A>G (p.Met2103Val)
NM_001271938.2(MEGF8):c.6359G>C (p.Gly2120Ala)
NM_001271938.2(MEGF8):c.6533C>G (p.Pro2178Arg) rs575829700
NM_001271938.2(MEGF8):c.6688G>A (p.Gly2230Ser)
NM_001271938.2(MEGF8):c.6715C>T (p.Arg2239Cys) rs1174809027
NM_001271938.2(MEGF8):c.6716G>A (p.Arg2239His)
NM_001271938.2(MEGF8):c.7003G>A (p.Glu2335Lys) rs2147509511
NM_001271938.2(MEGF8):c.7327C>T (p.Arg2443Cys)
NM_001271938.2(MEGF8):c.7621G>A (p.Gly2541Ser)
NM_001271938.2(MEGF8):c.7774G>T (p.Val2592Leu) rs148860986
NM_001271938.2(MEGF8):c.7786C>A (p.Leu2596Met) rs140517402
NM_001271938.2(MEGF8):c.7855G>A (p.Val2619Met)
NM_001271938.2(MEGF8):c.828+23G>A
NM_001271938.2(MEGF8):c.8381C>G (p.Pro2794Arg) rs2147521192

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