ClinVar Miner

List of variants in gene MET reported as not provided

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Gene type:
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Total variants: 30
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HGVS dbSNP
NM_001127500.3(MET):c.-14-3297G>C rs80048442
NM_001127500.3(MET):c.-14-3314A>T rs80153920
NM_001127500.3(MET):c.1039G>A (p.Ala347Thr) rs200074800
NM_001127500.3(MET):c.103A>T (p.Met35Leu) rs375353223
NM_001127500.3(MET):c.1085T>C (p.Met362Thr) rs77523018
NM_001127500.3(MET):c.110T>C (p.Val37Ala) rs201315884
NM_001127500.3(MET):c.1124A>G (p.Asn375Ser) rs33917957
NM_001127500.3(MET):c.1171G>A (p.Gly391Arg) rs587778443
NM_001127500.3(MET):c.1660G>A (p.Gly554Arg) rs200218511
NM_001127500.3(MET):c.1701+25A>G rs73469198
NM_001127500.3(MET):c.1701+58_1701+59insTG rs587777950
NM_001127500.3(MET):c.1701+75T>G rs553431706
NM_001127500.3(MET):c.1701+80dup rs587777951
NM_001127500.3(MET):c.1723C>A (p.Leu575Ile) rs587778445
NM_001127500.3(MET):c.1771C>T (p.Arg591Trp) rs45602940
NM_001127500.3(MET):c.1965+20A>G rs587777952
NM_001127500.3(MET):c.1972G>A (p.Val658Ile) rs587778446
NM_001127500.3(MET):c.2602A>G (p.Ile868Val) rs200524064
NM_001127500.3(MET):c.2716C>T (p.His906Tyr) rs115574135
NM_001127500.3(MET):c.289C>G (p.Pro97Ala) rs199736573
NM_001127500.3(MET):c.2962C>T (p.Arg988Cys) rs34589476
NM_001127500.3(MET):c.3029C>T (p.Thr1010Ile) rs56391007
NM_001127500.3(MET):c.3031A>G (p.Thr1011Ala) rs587778441
NM_001127500.3(MET):c.3576T>C (p.His1192=) rs146651797
NM_001127500.3(MET):c.4027G>A (p.Glu1343Lys) rs587778444
NM_001127500.3(MET):c.4141G>A (p.Ala1381Thr) rs45578433
NM_001127500.3(MET):c.504G>T (p.Glu168Asp) rs55985569
NM_001127500.3(MET):c.510C>G (p.Ser170Arg) rs587778442
NM_001127500.3(MET):c.71G>A (p.Gly24Glu) rs180985111
NM_001127500.3(MET):c.948A>G (p.Ile316Met) rs35225896

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