ClinVar Miner

List of variants in gene MET reported as uncertain significance for not specified

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Gene type:
ClinVar version:
Total variants: 66
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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.2908C>T (p.Arg970Cys) rs34589476 0.00327
NM_000245.4(MET):c.1715G>A (p.Ser572Asn) rs199771406 0.00188
NM_000245.4(MET):c.1039G>A (p.Ala347Thr) rs200074800 0.00068
NM_000245.4(MET):c.467C>T (p.Ser156Leu) rs56311081 0.00061
NM_000245.4(MET):c.406G>A (p.Val136Ile) rs199701987 0.00058
NM_000245.4(MET):c.71G>A (p.Gly24Glu) rs180985111 0.00055
NM_000245.4(MET):c.3521A>G (p.His1174Arg) rs372830789 0.00041
NM_000245.4(MET):c.901A>G (p.Thr301Ala) rs201687037 0.00038
NM_000245.4(MET):c.1076G>A (p.Arg359Gln) rs201274041 0.00022
NM_000245.4(MET):c.1412G>A (p.Gly471Glu) rs373312981 0.00016
NM_000245.4(MET):c.3236A>G (p.His1079Arg) rs758292223 0.00009
NM_000245.4(MET):c.3497G>A (p.Arg1166Gln) rs199763277 0.00008
NM_000245.4(MET):c.3811G>A (p.Val1271Met) rs751186512 0.00006
NM_000245.4(MET):c.100G>A (p.Glu34Lys) rs764246939 0.00005
NM_000245.4(MET):c.1063G>A (p.Glu355Lys) rs561295443 0.00005
NM_000245.4(MET):c.4007G>A (p.Arg1336Gln) rs369312680 0.00005
NM_000245.4(MET):c.632T>G (p.Leu211Trp) rs45483396 0.00005
NM_000245.4(MET):c.2677T>A (p.Leu893Ile) rs376104371 0.00004
NM_000245.4(MET):c.2909G>A (p.Arg970His) rs45607832 0.00004
NM_000245.4(MET):c.4034T>C (p.Ile1345Thr) rs768188910 0.00004
NM_000245.4(MET):c.2555T>A (p.Met852Lys) rs369758288 0.00003
NM_000245.4(MET):c.3230T>C (p.Ile1077Thr) rs1177400289 0.00003
NM_000245.4(MET):c.1343G>A (p.Gly448Glu) rs750256779 0.00002
NM_000245.4(MET):c.2216G>A (p.Arg739His) rs45553236 0.00002
NM_000245.4(MET):c.2755G>A (p.Val919Ile) rs759522148 0.00002
NM_000245.4(MET):c.4145G>A (p.Arg1382Gln) rs752694306 0.00002
NM_000245.4(MET):c.1451A>G (p.His484Arg) rs781545528 0.00001
NM_000245.4(MET):c.249G>C (p.Glu83Asp) rs751158831 0.00001
NM_000245.4(MET):c.2851T>C (p.Phe951Leu) rs756670611 0.00001
NM_000245.4(MET):c.3509G>A (p.Arg1170Gln) rs369838973 0.00001
NM_000245.4(MET):c.490C>G (p.Pro164Ala) rs765759353 0.00001
NM_000245.4(MET):c.689C>T (p.Thr230Met) rs587780740 0.00001
NM_000245.4(MET):c.1127A>G (p.Lys376Arg)
NM_000245.4(MET):c.1174C>A (p.Pro392Thr) rs886061943
NM_000245.4(MET):c.1276C>T (p.Arg426Cys) rs774779741
NM_000245.4(MET):c.1285T>A (p.Leu429Ile) rs911380470
NM_000245.4(MET):c.1306G>C (p.Glu436Gln) rs200740468
NM_000245.4(MET):c.1354A>G (p.Ile452Val) rs1793018926
NM_000245.4(MET):c.1363C>T (p.Leu455Phe) rs780077898
NM_000245.4(MET):c.1702-24A>T
NM_000245.4(MET):c.1838C>T (p.Thr613Ile)
NM_000245.4(MET):c.1910C>A (p.Ser637Tyr) rs2116920387
NM_000245.4(MET):c.2209A>G (p.Ser737Gly) rs755571526
NM_000245.4(MET):c.2285G>A (p.Gly762Asp) rs1060503541
NM_000245.4(MET):c.2434C>G (p.Gln812Glu) rs398123568
NM_000245.4(MET):c.2510A>G (p.His837Arg) rs1041349799
NM_000245.4(MET):c.253A>G (p.Lys85Glu) rs1791469321
NM_000245.4(MET):c.2959C>G (p.Arg987Gly)
NM_000245.4(MET):c.3041A>G (p.Asn1014Ser) rs2117029538
NM_000245.4(MET):c.3151G>A (p.Val1051Ile) rs775997318
NM_000245.4(MET):c.3281A>C (p.His1094Pro) rs121913243
NM_000245.4(MET):c.3286A>G (p.Thr1096Ala) rs2117039915
NM_000245.4(MET):c.3317A>G (p.His1106Arg)
NM_000245.4(MET):c.356C>A (p.Ala119Asp)
NM_000245.4(MET):c.3593A>G (p.Lys1198Arg) rs2117060321
NM_000245.4(MET):c.3658G>C (p.Val1220Leu) rs121913670
NM_000245.4(MET):c.3775_3776del (p.Lys1259fs) rs2117067376
NM_000245.4(MET):c.3936-13_3936-10del rs745366999
NM_000245.4(MET):c.4052A>G (p.His1351Arg) rs1490801483
NM_000245.4(MET):c.4097C>T (p.Pro1366Leu) rs778084120
NM_000245.4(MET):c.4144C>T (p.Arg1382Ter) rs200315561
NM_000245.4(MET):c.452C>T (p.Thr151Ile) rs1584876832
NM_000245.4(MET):c.751C>G (p.His251Asp)
NM_000245.4(MET):c.799G>A (p.Glu267Lys) rs755954919
NM_000245.4(MET):c.955G>T (p.Ala319Ser) rs545332056

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