ClinVar Miner

List of variants in gene MET reported as benign for renal cell adenocarcinoma

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.*1428G>A rs1621 0.63315
NM_000245.4(MET):c.*2240G>A rs6566 0.34157
NM_000245.4(MET):c.4092G>A (p.Pro1364=) rs41737 0.34093
NM_000245.4(MET):c.*1028A>G rs41738 0.34071
NM_000245.4(MET):c.4017G>A (p.Ala1339=) rs2023748 0.34017
NM_000245.4(MET):c.*1326A>G rs41739 0.34010
NM_000245.4(MET):c.3858C>T (p.Asp1286=) rs41736 0.33828
NM_000245.4(MET):c.1944A>G (p.Gln648=) rs13223756 0.16754
NM_000245.4(MET):c.534C>T (p.Ser178=) rs35775721 0.07211
NM_000245.4(MET):c.*684G>A rs12540703 0.05662
NM_000245.4(MET):c.1131C>T (p.Ile377=) rs28444388 0.05590
NM_000245.4(MET):c.144G>A (p.Ala48=) rs11762213 0.03399
NM_000245.4(MET):c.*216C>A rs149188493 0.02223
NM_000245.4(MET):c.1124A>G (p.Asn375Ser) rs33917957 0.01723
NM_000245.4(MET):c.-14-13C>T rs36080330 0.00978
NM_000245.4(MET):c.2975C>T (p.Thr992Ile) rs56391007 0.00911
NM_000245.4(MET):c.1085T>C (p.Met362Thr) rs77523018 0.00742
NM_000245.4(MET):c.390C>T (p.Leu130=) rs150588908 0.00740
NM_000245.4(MET):c.948A>G (p.Ile316Met) rs35225896 0.00641
NM_000245.4(MET):c.*2202G>A rs14456 0.00515
NM_000245.4(MET):c.*1987C>T rs76322625 0.00499
NM_000245.4(MET):c.504G>T (p.Glu168Asp) rs55985569 0.00420
NM_000245.4(MET):c.*1220G>A rs139535303 0.00336
NM_000245.4(MET):c.-14-4G>A rs144126521 0.00331
NM_000245.4(MET):c.2908C>T (p.Arg970Cys) rs34589476 0.00327
NM_000245.4(MET):c.*787G>A rs143472935 0.00290
NM_000245.4(MET):c.*231T>G rs59399612 0.00287
NM_000245.4(MET):c.*1010G>T rs150534017 0.00272
NM_000245.4(MET):c.*87G>A rs41281081 0.00250
NM_000245.4(MET):c.3522T>C (p.His1174=) rs146651797 0.00243
NM_000245.4(MET):c.*385G>A rs181068390 0.00235
NM_000245.4(MET):c.*201C>T rs1129355 0.00192
NM_000245.4(MET):c.1715G>A (p.Ser572Asn) rs199771406 0.00188
NM_000245.4(MET):c.*2100C>T rs190739281 0.00165
NM_000245.4(MET):c.*1871G>A rs139377965 0.00152
NM_000245.4(MET):c.*1224C>T rs149713628 0.00150
NM_000245.4(MET):c.*656G>A rs531456758 0.00104
NM_000245.4(MET):c.*602C>T rs147343288 0.00093
NM_000245.4(MET):c.*944A>G rs565768785 0.00076
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.467C>T (p.Ser156Leu) rs56311081 0.00061
NM_000245.4(MET):c.406G>A (p.Val136Ile) rs199701987 0.00058
NM_000245.4(MET):c.3523-12C>G rs186524917 0.00053
NM_000245.4(MET):c.3810C>T (p.Gly1270=) rs200865810 0.00039
NM_000245.4(MET):c.1191C>T (p.Cys397=) rs35763409 0.00028
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.1263C>T (p.Thr421=) rs45499391 0.00016
NM_000245.4(MET):c.4087G>A (p.Ala1363Thr) rs45578433 0.00016
NM_000245.4(MET):c.110T>C (p.Val37Ala) rs201315884 0.00009
NM_000245.4(MET):c.960G>A (p.Ala320=) rs191198682 0.00007
NM_000245.4(MET):c.36C>T (p.Leu12=) rs188625702 0.00006
NM_000245.4(MET):c.4075G>A (p.Val1359Ile) rs752669237 0.00006
NM_000245.4(MET):c.3065G>A (p.Arg1022Gln) rs45612435 0.00005
NM_000245.4(MET):c.*397A>G rs559231345 0.00003
NM_000245.4(MET):c.690G>A (p.Thr230=) rs200138253 0.00003
NM_000245.4(MET):c.1965+14T>C rs543293293 0.00002
NM_000245.4(MET):c.*1233G>A rs560568639
NM_000245.4(MET):c.*1244G>A rs144559852
NM_000245.4(MET):c.*376G>T rs553602374
NM_000245.4(MET):c.1701+58dup rs112241458
NM_000245.4(MET):c.1701+59G>T rs759007523
NM_000245.4(MET):c.2584-9del rs57349036

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