ClinVar Miner

List of variants in gene MET reported as uncertain significance by Quest Diagnostics Nichols Institute San Juan Capistrano

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Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.901A>G (p.Thr301Ala) rs201687037 0.00038
NM_000245.4(MET):c.2198C>T (p.Thr733Ile) rs201271860 0.00029
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.1771C>T (p.Arg591Trp) rs45602940 0.00015
NM_000245.4(MET):c.40C>T (p.Leu14Phe) rs763344951 0.00015
NM_000245.4(MET):c.1975A>T (p.Ile659Leu) rs753958204 0.00014
NM_000245.4(MET):c.289C>G (p.Pro97Ala) rs199736573 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.2318C>T (p.Pro773Leu) rs771333219 0.00009
NM_000245.4(MET):c.3236A>G (p.His1079Arg) rs758292223 0.00009
NM_000245.4(MET):c.1669A>G (p.Thr557Ala) rs374733251 0.00008
NM_000245.4(MET):c.2543T>C (p.Val848Ala) rs587782205 0.00008
NM_000245.4(MET):c.3497G>A (p.Arg1166Gln) rs199763277 0.00008
NM_000245.4(MET):c.1862C>T (p.Thr621Ile) rs375951814 0.00007
NM_000245.4(MET):c.3218C>T (p.Pro1073Leu) rs370529693 0.00007
NM_000245.4(MET):c.105G>C (p.Met35Ile) rs376244358 0.00006
NM_000245.4(MET):c.4075G>A (p.Val1359Ile) rs752669237 0.00006
NM_000245.4(MET):c.1063G>A (p.Glu355Lys) rs561295443 0.00005
NM_000245.4(MET):c.1988C>T (p.Ser663Leu) rs376459715 0.00005
NM_000245.4(MET):c.142G>A (p.Ala48Thr) rs374050750 0.00004
NM_000245.4(MET):c.3118T>C (p.Ser1040Pro) rs771328219 0.00004
NM_000245.4(MET):c.1853C>T (p.Thr618Met) rs753407699 0.00003
NM_000245.4(MET):c.1972G>A (p.Val658Ile) rs587778446 0.00003
NM_000245.4(MET):c.2555T>A (p.Met852Lys) rs369758288 0.00003
NM_000245.4(MET):c.4117G>C (p.Asp1373His) rs398123570 0.00003
NM_000245.4(MET):c.617T>C (p.Phe206Ser) rs746295363 0.00003
NM_000245.4(MET):c.762A>C (p.Glu254Asp) rs760278126 0.00003
NM_000245.4(MET):c.1640G>A (p.Arg547Gln) rs761951444 0.00002
NM_000245.4(MET):c.1749A>G (p.Ile583Met) rs776805376 0.00002
NM_000245.4(MET):c.2326G>C (p.Val776Leu) rs771976817 0.00002
NM_000245.4(MET):c.535G>A (p.Ala179Thr) rs753697730 0.00002
NM_000245.4(MET):c.1099A>G (p.Ile367Val) rs774146015 0.00001
NM_000245.4(MET):c.1171G>A (p.Gly391Arg) rs587778443 0.00001
NM_000245.4(MET):c.1477G>C (p.Glu493Gln) rs965319455 0.00001
NM_000245.4(MET):c.1660G>A (p.Gly554Arg) rs200218511 0.00001
NM_000245.4(MET):c.1937C>A (p.Thr646Lys) rs751307227 0.00001
NM_000245.4(MET):c.2073A>G (p.Ser691=) rs765318603 0.00001
NM_000245.4(MET):c.2381C>G (p.Ser794Cys) rs371939364 0.00001
NM_000245.4(MET):c.2496T>C (p.Asp832=) rs769035394 0.00001
NM_000245.4(MET):c.255G>A (p.Lys85=) rs1327946446 0.00001
NM_000245.4(MET):c.2851T>C (p.Phe951Leu) rs756670611 0.00001
NM_000245.4(MET):c.331G>A (p.Val111Ile) rs368750834 0.00001
NM_000245.4(MET):c.3509G>A (p.Arg1170Gln) rs369838973 0.00001
NM_000245.4(MET):c.3586G>A (p.Ala1196Thr) rs970206545 0.00001
NM_000245.4(MET):c.3727G>A (p.Ala1243Thr) rs752351789 0.00001
NM_000245.4(MET):c.3997C>G (p.Leu1333Val) rs758738756 0.00001
NM_000245.4(MET):c.716C>T (p.Pro239Leu) rs45551737 0.00001
NM_000245.4(MET):c.1052C>T (p.Pro351Leu)
NM_000245.4(MET):c.1056T>C (p.Asp352=)
NM_000245.4(MET):c.1157T>G (p.Leu386Arg) rs1554379180
NM_000245.4(MET):c.1274A>G (p.Gln425Arg) rs1793013042
NM_000245.4(MET):c.1411G>A (p.Gly471Arg) rs1207715563
NM_000245.4(MET):c.1472T>C (p.Ile491Thr) rs561588772
NM_000245.4(MET):c.1483A>G (p.Thr495Ala)
NM_000245.4(MET):c.1712A>G (p.Asn571Ser)
NM_000245.4(MET):c.2347G>C (p.Gly783Arg) rs879254334
NM_000245.4(MET):c.2557G>A (p.Gly853Ser) rs45575240
NM_000245.4(MET):c.2619A>G (p.Glu873=)
NM_000245.4(MET):c.2630T>C (p.Val877Ala)
NM_000245.4(MET):c.2846T>A (p.Leu949His)
NM_000245.4(MET):c.3301G>A (p.Asp1101Asn) rs749678495
NM_000245.4(MET):c.3936-8T>C
NM_000245.4(MET):c.4135G>A (p.Val1379Met) rs1554402266
NM_000245.4(MET):c.4141A>G (p.Thr1381Ala) rs1292389793
NM_000245.4(MET):c.481A>C (p.Ile161Leu)
NM_000245.4(MET):c.491C>T (p.Pro164Leu) rs1562883575
NM_000245.4(MET):c.850A>G (p.Ile284Val) rs776014448
NM_000245.4(MET):c.86C>A (p.Ala29Glu)
NM_000245.4(MET):c.943A>G (p.Asn315Asp)
NM_000245.4(MET):c.950T>C (p.Leu317Pro)
Single allele

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