List of variants in gene MET reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 37

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HGVS	dbSNP	gnomAD frequency
NM_000245.4(MET):c.1702-152C>T	rs38860	0.96352
NM_000245.4(MET):c.3523-75T>C	rs6947629	0.66316
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.3799-293G>A	rs41735	0.33882
NM_000245.4(MET):c.3858C>T (p.Asp1286=)	rs41736	0.33828
NM_000245.4(MET):c.2265-314G>A	rs10215153	0.32195
NM_000245.4(MET):c.1200+193_1200+194insT	rs35212357	0.23883
NM_000245.4(MET):c.1200+244A>C	rs17138937	0.23872
NM_000245.4(MET):c.1944A>G (p.Gln648=)	rs13223756	0.16754
NM_000245.4(MET):c.3633-197G>A	rs2073560	0.13967
NM_000245.4(MET):c.534C>T (p.Ser178=)	rs35775721	0.07211
NM_000245.4(MET):c.2264+89C>T	rs17138978	0.05671
NM_000245.4(MET):c.1131C>T (p.Ile377=)	rs28444388	0.05590
NM_000245.4(MET):c.1201-247T>C	rs7804778	0.04313
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.2888-54_2888-53dup	rs140824245	0.03089
NM_000245.4(MET):c.1392+276G>C	rs10244916	0.03074
NM_000245.4(MET):c.3523-217T>A	rs73471132	0.02763
NM_000245.4(MET):c.3633-38A>G	rs115240747	0.02393
NM_000245.4(MET):c.*216C>A	rs149188493	0.02223
NM_000245.4(MET):c.3632+63C>T	rs6966012	0.02208
NM_000245.4(MET):c.3523-163G>A	rs138238598	0.02023
NM_000245.4(MET):c.2887+70G>A	rs6978257	0.01964
NM_000245.4(MET):c.3522+251T>C	rs73716771	0.01904
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.2908C>T (p.Arg970Cys)	rs34589476	0.00327
NM_000245.4(MET):c.1701+58dup	rs112241458
NM_000245.4(MET):c.2584-9del	rs57349036
NM_000245.4(MET):c.3523-241C>T	rs73471130

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