ClinVar Miner

List of variants in gene MET reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.4092G>A (p.Pro1364=) rs41737 0.34093
NM_000245.4(MET):c.4017G>A (p.Ala1339=) rs2023748 0.34017
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.1131C>T (p.Ile377=) rs28444388 0.05590
NM_000245.4(MET):c.144G>A (p.Ala48=) rs11762213 0.03399
NM_000245.4(MET):c.1124A>G (p.Asn375Ser) rs33917957 0.01723
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.-14-4G>A rs144126521 0.00331
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.2662C>T (p.His888Tyr) rs115574135 0.00166
NM_000245.4(MET):c.3549C>T (p.Gly1183=) rs371165052 0.00074
NM_000245.4(MET):c.798G>A (p.Arg266=) rs185301166 0.00073
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.959C>T (p.Ala320Val) rs35776110 0.00045
NM_000245.4(MET):c.2715C>T (p.Ser905=) rs45572835 0.00039
NM_000245.4(MET):c.2198C>T (p.Thr733Ile) rs201271860 0.00029
NM_000245.4(MET):c.1191C>T (p.Cys397=) rs35763409 0.00028
NM_000245.4(MET):c.1932C>T (p.His644=) rs45520237 0.00024
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.4087G>A (p.Ala1363Thr) rs45578433 0.00016
NM_000245.4(MET):c.1771C>T (p.Arg591Trp) rs45602940 0.00015
NM_000245.4(MET):c.1233G>A (p.Ala411=) rs374081963 0.00014
NM_000245.4(MET):c.1270T>C (p.Leu424=) rs372229471 0.00014
NM_000245.4(MET):c.289C>G (p.Pro97Ala) rs199736573 0.00012
NM_000245.4(MET):c.3798+5T>C rs368150874 0.00012
NM_000245.4(MET):c.2684C>T (p.Thr895Met) rs199502137 0.00011
NM_000245.4(MET):c.2110A>G (p.Asn704Asp) rs373030463 0.00010
NM_000245.4(MET):c.1669A>G (p.Thr557Ala) rs374733251 0.00008
NM_000245.4(MET):c.12C>T (p.Pro4=) rs772251895 0.00006
NM_000245.4(MET):c.4134G>A (p.Glu1378=) rs879254328 0.00006
NM_000245.4(MET):c.1019A>G (p.Asp340Gly) rs200690492 0.00004
NM_000245.4(MET):c.1392+14G>A rs529823741 0.00004
NM_000245.4(MET):c.2913C>T (p.Tyr971=) rs371379572 0.00004
NM_000245.4(MET):c.341A>T (p.Asp114Val) rs773659883 0.00004
NM_000245.4(MET):c.3459G>A (p.Pro1153=) rs201245213 0.00004
NM_000245.4(MET):c.3489A>T (p.Gly1163=) rs753101831 0.00004
NM_000245.4(MET):c.1279G>A (p.Val427Ile) rs376364468 0.00003
NM_000245.4(MET):c.1723C>A (p.Leu575Ile) rs587778445 0.00003
NM_000245.4(MET):c.690G>A (p.Thr230=) rs200138253 0.00003
NM_000245.4(MET):c.762A>C (p.Glu254Asp) rs760278126 0.00003
NM_000245.4(MET):c.900C>G (p.Leu300=) rs540354779 0.00003
NM_000245.4(MET):c.2319G>A (p.Pro773=) rs141733128 0.00002
NM_000245.4(MET):c.3378C>T (p.Thr1126=) rs201111132 0.00002
NM_000245.4(MET):c.3702C>T (p.Tyr1234=) rs201747580 0.00002
NM_000245.4(MET):c.146A>G (p.Glu49Gly) rs370499060 0.00001
NM_000245.4(MET):c.1719A>G (p.Ala573=) rs199776656 0.00001
NM_000245.4(MET):c.2303A>G (p.Asn768Ser) rs749126070 0.00001
NM_000245.4(MET):c.241G>T (p.Val81Phe) rs757883355 0.00001
NM_000245.4(MET):c.2802G>C (p.Leu934Phe) rs1361155132 0.00001
NM_000245.4(MET):c.3281A>G (p.His1094Arg) rs121913243 0.00001
NM_000245.4(MET):c.3377C>A (p.Thr1126Asn) rs367634278 0.00001
NM_000245.4(MET):c.3684C>T (p.Asp1228=) rs786201612 0.00001
NM_000245.4(MET):c.3859G>A (p.Val1287Ile) rs780102059 0.00001
NM_000245.4(MET):c.3864C>T (p.Asn1288=) rs768627036 0.00001
NM_000245.4(MET):c.4008G>A (p.Arg1336=) rs373857586 0.00001
NM_000245.4(MET):c.405C>T (p.Ser135=) rs200494620 0.00001
NM_000245.4(MET):c.1051C>G (p.Pro351Ala) rs587782807
NM_000245.4(MET):c.1276C>A (p.Arg426Ser)
NM_000245.4(MET):c.1647G>A (p.Glu549=) rs1584923365
NM_000245.4(MET):c.1863-5dup rs766900241
NM_000245.4(MET):c.2169A>G (p.Lys723=)
NM_000245.4(MET):c.2375A>C (p.His792Pro) rs980467681
NM_000245.4(MET):c.2584-10_2584-9dup
NM_000245.4(MET):c.2584-4T>C rs1554397896
NM_000245.4(MET):c.2663A>G (p.His888Arg) rs1584953276
NM_000245.4(MET):c.2790T>C (p.Asn930=) rs933744184
NM_000245.4(MET):c.3203A>G (p.His1068Arg)
NM_000245.4(MET):c.3478A>G (p.Met1160Val) rs1554399597
NM_000245.4(MET):c.3804C>T (p.Ser1268=) rs764822445
NM_000245.4(MET):c.3807T>C (p.Phe1269=) rs1554402156
NM_000245.4(MET):c.3915C>T (p.Pro1305=) rs555099334
NM_000245.4(MET):c.4038G>A (p.Gly1346=) rs886038413
NM_000245.4(MET):c.713T>C (p.Leu238Ser) rs34349517
NM_000245.4(MET):c.732T>G (p.Ser244=) rs770202229

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