ClinVar Miner

List of variants in gene MET reported as not provided by ITMI

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Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.-14-3314A>T rs80153920 0.05896
NM_000245.4(MET):c.1701+25A>G rs73469198 0.03101
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.948A>G (p.Ile316Met) rs35225896 0.00641
NM_000245.4(MET):c.504G>T (p.Glu168Asp) rs55985569 0.00420
NM_000245.4(MET):c.1701+75T>G rs553431706 0.00407
NM_000245.4(MET):c.2908C>T (p.Arg970Cys) rs34589476 0.00327
NM_000245.4(MET):c.3522T>C (p.His1174=) rs146651797 0.00243
NM_000245.4(MET):c.2662C>T (p.His888Tyr) rs115574135 0.00166
NM_000245.4(MET):c.1039G>A (p.Ala347Thr) rs200074800 0.00068
NM_000245.4(MET):c.71G>A (p.Gly24Glu) rs180985111 0.00055
NM_000245.4(MET):c.103A>T (p.Met35Leu) rs375353223 0.00041
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.289C>G (p.Pro97Ala) rs199736573 0.00012
NM_000245.4(MET):c.2548A>G (p.Ile850Val) rs200524064 0.00011
NM_000245.4(MET):c.110T>C (p.Val37Ala) rs201315884 0.00009
NM_000245.4(MET):c.510C>G (p.Ser170Arg) rs587778442 0.00004
NM_000245.4(MET):c.1723C>A (p.Leu575Ile) rs587778445 0.00003
NM_000245.4(MET):c.1972G>A (p.Val658Ile) rs587778446 0.00003
NM_000245.4(MET):c.1171G>A (p.Gly391Arg) rs587778443 0.00001
NM_000245.4(MET):c.1660G>A (p.Gly554Arg) rs200218511 0.00001
NM_000245.4(MET):c.2977A>G (p.Thr993Ala) rs587778441 0.00001
NM_000245.4(MET):c.3973G>A (p.Glu1325Lys) rs587778444 0.00001
NM_000245.4(MET):c.-14-3297G>C rs80048442
NM_000245.4(MET):c.1701+58_1701+59insTG rs587777950
NM_000245.4(MET):c.1701+80dup rs587777951
NM_000245.4(MET):c.1965+20A>G rs587777952

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