ClinVar Miner

List of variants in gene MET reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.*1886T>A rs536185931 0.00076
NM_000245.4(MET):c.*1636C>T rs186175651 0.00057
NM_000245.4(MET):c.*1637G>A rs534514626 0.00026
NM_000245.4(MET):c.*655C>T rs563978117 0.00026
NM_000245.4(MET):c.*2079G>A rs757859772 0.00024
NM_000245.4(MET):c.*1784T>A rs554029534 0.00023
NM_000245.4(MET):c.*1593G>A rs764929802 0.00020
NM_000245.4(MET):c.*1714C>A rs747850853 0.00009
NM_000245.4(MET):c.*1878A>G rs770910579 0.00007
NM_000245.4(MET):c.*803T>A rs1001801655 0.00006
NM_000245.4(MET):c.*221G>A rs886061946 0.00004
NM_000245.4(MET):c.*76C>T rs527496385 0.00004
NM_000245.4(MET):c.1320A>G (p.Thr440=) rs763726060 0.00004
NM_000245.4(MET):c.2909G>A (p.Arg970His) rs45607832 0.00004
NM_000245.4(MET):c.341A>T (p.Asp114Val) rs773659883 0.00004
NM_000245.4(MET):c.*2051C>T rs886061951 0.00003
NM_000245.4(MET):c.*296G>C rs1237383281 0.00003
NM_000245.4(MET):c.2971C>T (p.Pro991Ser) rs768678989 0.00003
NM_000245.4(MET):c.788C>T (p.Thr263Met) rs764052874 0.00003
NM_000245.4(MET):c.*530G>A rs185897782 0.00002
NM_000245.4(MET):c.4074C>T (p.Asn1358=) rs772860611 0.00002
NM_000245.4(MET):c.*1477C>T rs750893461 0.00001
NM_000245.4(MET):c.*41A>G rs771518812 0.00001
NM_000245.4(MET):c.1693A>G (p.Ile565Val) rs745479104 0.00001
NM_000245.4(MET):c.2673C>T (p.Ala891=) rs561131509 0.00001
NM_000245.4(MET):c.3091A>G (p.Met1031Val) rs45564937 0.00001
NM_000245.4(MET):c.600C>G (p.Thr200=) rs1225303075 0.00001
NM_000245.4(MET):c.*105C>A rs886061945
NM_000245.4(MET):c.*1244G>T rs144559852
NM_000245.4(MET):c.*1359T>C rs1795712500
NM_000245.4(MET):c.*1460C>G rs886061949
NM_000245.4(MET):c.*1809C>T rs868554436
NM_000245.4(MET):c.*1882G>T rs886061950
NM_000245.4(MET):c.*1909A>G rs1795730503
NM_000245.4(MET):c.*1929A>G rs1321841621
NM_000245.4(MET):c.*2134T>A rs144156652
NM_000245.4(MET):c.*2147T>C rs1795737615
NM_000245.4(MET):c.*2202G>T rs14456
NM_000245.4(MET):c.*2245G>T rs1447240969
NM_000245.4(MET):c.*27C>A rs1795669540
NM_000245.4(MET):c.*2G>T rs1795668471
NM_000245.4(MET):c.*359G>A rs1795682838
NM_000245.4(MET):c.*422T>A rs886061947
NM_000245.4(MET):c.*438T>A rs955990225
NM_000245.4(MET):c.*480T>C rs1207133647
NM_000245.4(MET):c.*493A>C rs1795687373
NM_000245.4(MET):c.*786C>T rs935854365
NM_000245.4(MET):c.*984C>T rs573510587
NM_000245.4(MET):c.*995G>T rs886061948
NM_000245.4(MET):c.1011G>A (p.Leu337=) rs886061942
NM_000245.4(MET):c.1174C>A (p.Pro392Thr) rs886061943
NM_000245.4(MET):c.1484C>G (p.Thr495Arg) rs45585831
NM_000245.4(MET):c.1489A>G (p.Asn497Asp) rs766209435
NM_000245.4(MET):c.1863-5dup rs766900241
NM_000245.4(MET):c.1965+11T>G rs780230492
NM_000245.4(MET):c.2510A>G (p.His837Arg) rs1041349799
NM_000245.4(MET):c.3065G>T (p.Arg1022Leu) rs45612435
NM_000245.4(MET):c.3246A>T (p.Glu1082Asp) rs1794955289
NM_000245.4(MET):c.367G>A (p.Asp123Asn) rs760106468
NM_000245.4(MET):c.847T>C (p.Ser283Pro) rs1791505194

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