ClinVar Miner

List of variants in gene MET reported by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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Total variants: 24
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HGVS dbSNP gnomAD frequency
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.948A>G (p.Ile316Met) rs35225896 0.00641
NM_000245.4(MET):c.504G>T (p.Glu168Asp) rs55985569 0.00420
NM_000245.4(MET):c.2908C>T (p.Arg970Cys) rs34589476 0.00327
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.110T>C (p.Val37Ala) rs201315884 0.00009
NM_000245.4(MET):c.1019A>G (p.Asp340Gly) rs200690492 0.00004
NM_000245.4(MET):c.1810C>G (p.Leu604Val) rs201861645 0.00003
NM_000245.4(MET):c.3356G>C (p.Gly1119Ala) rs201037977 0.00003
NM_000245.4(MET):c.1232C>T (p.Ala411Val) rs201154533 0.00001
NM_000245.4(MET):c.199A>G (p.Thr67Ala) rs202047059 0.00001
NM_000245.4(MET):c.4151C>G (p.Ala1384Gly) rs202166889 0.00001
NM_000245.2:c.-14-3312A>T
NM_000245.4(MET):c.1048A>C (p.Lys350Gln) rs201191014
NM_000245.4(MET):c.1180C>A (p.His394Asn) rs201628326
NM_000245.4(MET):c.1237C>A (p.Arg413Ser) rs201980687
NM_000245.4(MET):c.1292T>C (p.Met431Thr) rs201789039
NM_000245.4(MET):c.1304G>A (p.Ser435Asn) rs199761604
NM_000245.4(MET):c.1306G>C (p.Glu436Gln) rs200740468
NM_000245.4(MET):c.1345G>A (p.Asp449Asn) rs200819547
NM_000245.4(MET):c.1392+5G>A rs386833405
NM_000245.4(MET):c.2383A>G (p.Asn795Asp) rs200633053

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