ClinVar Miner

List of variants in gene MET reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 39
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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.1701+25A>G rs73469198 0.03101
NM_000245.4(MET):c.3633-38A>G rs115240747 0.02393
NM_000245.4(MET):c.1124A>G (p.Asn375Ser) rs33917957 0.01723
NM_000245.4(MET):c.-14-13C>T rs36080330 0.00978
NM_000245.4(MET):c.2888-36G>A rs35624294 0.00931
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.504G>T (p.Glu168Asp) rs55985569 0.00420
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.654G>A (p.Arg218=) rs35284565 0.00153
NM_000245.4(MET):c.3523-12C>G rs186524917 0.00053
NM_000245.4(MET):c.607T>A (p.Ser203Thr) rs200861145 0.00053
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.3054C>T (p.Asn1018=) rs369148519 0.00002
NM_000245.4(MET):c.1393-6G>A rs202194405 0.00001
NM_000245.4(MET):c.1528-39_1528-38delinsAT rs1554391208
NM_000245.4(MET):c.1701+57_1701+58dup rs112241458
NM_000245.4(MET):c.1701+58del rs112241458
NM_000245.4(MET):c.1701+58dup rs112241458
NM_000245.4(MET):c.2584-10_2584-9del rs57349036
NM_000245.4(MET):c.2584-11_2584-9del
NM_000245.4(MET):c.2584-7del rs587780736
NM_000245.4(MET):c.2584-9del rs57349036
NM_000245.4(MET):c.2584-9dup rs57349036
NM_000245.4(MET):c.3804C>T (p.Ser1268=) rs764822445
NM_000245.4(MET):c.3936-13_3936-10del rs745366999
NM_000245.4(MET):c.4038G>A (p.Gly1346=) rs886038413

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