List of variants in gene MET reported as benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 20

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HGVS	dbSNP	gnomAD frequency
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.-14-4G>A	rs144126521	0.00331
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.2584-9del	rs57349036
NM_000245.4(MET):c.2584-9dup	rs57349036

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