ClinVar Miner

List of variants in gene MET reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 89
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.504G>T (p.Glu168Asp) rs55985569 0.00420
NM_000245.4(MET):c.2584-23T>A rs201491944 0.00247
NM_000245.4(MET):c.3522T>C (p.His1174=) rs146651797 0.00243
NM_000245.4(MET):c.2365-21G>C rs140853140 0.00242
NM_000245.4(MET):c.1715G>A (p.Ser572Asn) rs199771406 0.00188
NM_000245.4(MET):c.2662C>T (p.His888Tyr) rs115574135 0.00166
NM_000245.4(MET):c.1528-38A>T rs574459492 0.00158
NM_000245.4(MET):c.1528-39T>A rs556216308 0.00158
NM_000245.4(MET):c.654G>A (p.Arg218=) rs35284565 0.00153
NM_000245.4(MET):c.2584-9T>C rs74994656 0.00119
NM_000245.4(MET):c.3549C>T (p.Gly1183=) rs371165052 0.00074
NM_000245.4(MET):c.1039G>A (p.Ala347Thr) rs200074800 0.00068
NM_000245.4(MET):c.3523-12C>G rs186524917 0.00053
NM_000245.4(MET):c.607T>A (p.Ser203Thr) rs200861145 0.00053
NM_000245.4(MET):c.3810C>T (p.Gly1270=) rs200865810 0.00039
NM_000245.4(MET):c.1966-17T>C rs555288487 0.00027
NM_000245.4(MET):c.967A>G (p.Ser323Gly) rs201467281 0.00024
NM_000245.4(MET):c.4105T>C (p.Leu1369=) rs45575438 0.00021
NM_000245.4(MET):c.3522+12G>T rs200624981 0.00019
NM_000245.4(MET):c.1201-14A>G rs762306750 0.00016
NM_000245.4(MET):c.4087G>A (p.Ala1363Thr) rs45578433 0.00016
NM_000245.4(MET):c.1966-32G>C rs564891216 0.00012
NM_000245.4(MET):c.3218C>T (p.Pro1073Leu) rs370529693 0.00007
NM_000245.4(MET):c.12C>T (p.Pro4=) rs772251895 0.00006
NM_000245.4(MET):c.3168T>C (p.Ser1056=) rs376069508 0.00006
NM_000245.4(MET):c.1278C>T (p.Arg426=) rs748508881 0.00004
NM_000245.4(MET):c.1374A>G (p.Ser458=) rs755165691 0.00004
NM_000245.4(MET):c.1392+14G>A rs529823741 0.00004
NM_000245.4(MET):c.2584-16T>C rs766575983 0.00004
NM_000245.4(MET):c.3459G>A (p.Pro1153=) rs201245213 0.00004
NM_000245.4(MET):c.1701+14A>G rs768638354 0.00003
NM_000245.4(MET):c.1701+47T>G rs754198809 0.00003
NM_000245.4(MET):c.666G>A (p.Thr222=) rs1444020594 0.00003
NM_000245.4(MET):c.1862+24T>A rs758246482 0.00002
NM_000245.4(MET):c.2319G>A (p.Pro773=) rs141733128 0.00002
NM_000245.4(MET):c.2888-41T>C rs775541395 0.00002
NM_000245.4(MET):c.1584A>G (p.Gln528=) rs55755322 0.00001
NM_000245.4(MET):c.1644G>A (p.Ser548=) rs750584257 0.00001
NM_000245.4(MET):c.2136A>G (p.Pro712=) rs774439479 0.00001
NM_000245.4(MET):c.2673C>T (p.Ala891=) rs561131509 0.00001
NM_000245.4(MET):c.3276A>T (p.Val1092=) rs757338659 0.00001
NM_000245.4(MET):c.3799-5A>G rs1340355638 0.00001
NM_000245.4(MET):c.3972C>T (p.Ala1324=) rs201519623 0.00001
NM_000245.4(MET):c.805C>T (p.Leu269=) rs781257386 0.00001
NM_000245.4(MET):c.912A>G (p.Arg304=) rs762885066 0.00001
NM_000245.4(MET):c.-14-12C>G
NM_000245.4(MET):c.-14-26C>T rs2116576794
NM_000245.4(MET):c.1200+46A>C
NM_000245.4(MET):c.1392+21del
NM_000245.4(MET):c.1393-23G>A
NM_000245.4(MET):c.1428T>C (p.His476=) rs1432416607
NM_000245.4(MET):c.1527+33G>A
NM_000245.4(MET):c.1650A>G (p.Glu550=) rs2116836870
NM_000245.4(MET):c.1701+56_1701+58del
NM_000245.4(MET):c.1701+56_1701+58dup
NM_000245.4(MET):c.1701+57_1701+58del rs112241458
NM_000245.4(MET):c.1702-25del
NM_000245.4(MET):c.1716T>C (p.Ser572=) rs1382410716
NM_000245.4(MET):c.1719A>C (p.Ala573=) rs199776656
NM_000245.4(MET):c.1863-11T>C rs2116919514
NM_000245.4(MET):c.1896G>A (p.Lys632=) rs749484691
NM_000245.4(MET):c.1966-23T>C
NM_000245.4(MET):c.1966-29A>T rs2116922475
NM_000245.4(MET):c.1966-36A>G
NM_000245.4(MET):c.2102+50G>C
NM_000245.4(MET):c.2364+39A>G
NM_000245.4(MET):c.2365-14G>A rs769247886
NM_000245.4(MET):c.2583+45T>G rs768994279
NM_000245.4(MET):c.2583+50G>T
NM_000245.4(MET):c.2584-7del rs587780736
NM_000245.4(MET):c.2694T>C (p.Asn898=)
NM_000245.4(MET):c.2887+49T>G
NM_000245.4(MET):c.2888-22C>T
NM_000245.4(MET):c.3028+18G>A
NM_000245.4(MET):c.3029-45T>C
NM_000245.4(MET):c.3260-43T>C
NM_000245.4(MET):c.3341-49A>G
NM_000245.4(MET):c.3399T>C (p.Asp1133=) rs2117046045
NM_000245.4(MET):c.3486T>C (p.His1162=) rs765565377
NM_000245.4(MET):c.3523-10T>C rs2117059286
NM_000245.4(MET):c.3523-48G>A
NM_000245.4(MET):c.3632+17C>G rs758230781
NM_000245.4(MET):c.3632+17C>T rs758230781
NM_000245.4(MET):c.369C>T (p.Asp123=) rs1417054613
NM_000245.4(MET):c.372C>G (p.Thr124=) rs574911056
NM_000245.4(MET):c.3798+34T>C
NM_000245.4(MET):c.3799-17G>A
NM_000245.4(MET):c.591A>G (p.Val197=)
NM_000245.4(MET):c.639G>C (p.Ser213=)

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