ClinVar Miner

List of variants in gene MET studied for Osteofibrous dysplasia; Papillary renal cell carcinoma type 1; Hepatocellular carcinoma; Autosomal recessive nonsyndromic hearing loss 97; Arthrogryposis, distal, IIa 11

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Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.144G>A (p.Ala48=) rs11762213 0.03399
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.654G>A (p.Arg218=) rs35284565 0.00153
NM_000245.4(MET):c.406G>A (p.Val136Ile) rs199701987 0.00058
NM_000245.4(MET):c.967A>G (p.Ser323Gly) rs201467281 0.00024
NM_000245.4(MET):c.1263C>T (p.Thr421=) rs45499391 0.00016
NM_000245.4(MET):c.1669A>G (p.Thr557Ala) rs374733251 0.00008
NM_000245.4(MET):c.3218C>T (p.Pro1073Leu) rs370529693 0.00007
NM_000245.4(MET):c.803C>T (p.Thr268Ile) rs757427533 0.00007
NM_000245.4(MET):c.632T>G (p.Leu211Trp) rs45483396 0.00005
NM_000245.4(MET):c.1132G>A (p.Val378Ile) rs749738523 0.00004
NM_000245.4(MET):c.1881T>C (p.Gly627=) rs200050499 0.00004
NM_000245.4(MET):c.2825C>T (p.Ser942Leu) rs375576430 0.00004
NM_000245.4(MET):c.1414C>T (p.Pro472Ser) rs376589619 0.00003
NM_000245.4(MET):c.1510G>T (p.Val504Phe) rs587780735 0.00003
NM_000245.4(MET):c.1853C>T (p.Thr618Met) rs753407699 0.00003
NM_000245.4(MET):c.617T>C (p.Phe206Ser) rs746295363 0.00003
NM_000245.4(MET):c.1640G>A (p.Arg547Gln) rs761951444 0.00002
NM_000245.4(MET):c.4145G>A (p.Arg1382Gln) rs752694306 0.00002
NM_000245.4(MET):c.1450C>T (p.His484Tyr) rs771272439 0.00001
NM_000245.4(MET):c.1477G>C (p.Glu493Gln) rs965319455 0.00001
NM_000245.4(MET):c.306C>G (p.Ser102Arg) rs749383450 0.00001
NM_000245.4(MET):c.3281A>G (p.His1094Arg) rs121913243 0.00001
NM_000245.4(MET):c.3403A>T (p.Ser1135Cys) rs1394199299 0.00001
NM_000245.4(MET):c.3509G>A (p.Arg1170Gln) rs369838973 0.00001
NM_000245.4(MET):c.362T>C (p.Val121Ala) rs879254339 0.00001
NM_000245.4(MET):c.3878C>G (p.Thr1293Ser) rs779121848 0.00001
NM_000245.4(MET):c.3973G>A (p.Glu1325Lys) rs587778444 0.00001
NM_000245.4(MET):c.4082G>A (p.Cys1361Tyr) rs766190061 0.00001
NM_000245.4(MET):c.4150G>A (p.Ala1384Thr) rs758486336 0.00001
NM_000245.4(MET):c.800A>G (p.Glu267Gly) rs751564290 0.00001
NM_000245.4(MET):c.1067del (p.Pro356fs)
NM_000245.4(MET):c.1285T>A (p.Leu429Ile) rs911380470
NM_000245.4(MET):c.2074A>G (p.Ile692Val)
NM_000245.4(MET):c.2253A>T (p.Lys751Asn)
NM_000245.4(MET):c.2265-41G>C
NM_000245.4(MET):c.2363T>C (p.Val788Ala) rs786204142
NM_000245.4(MET):c.2766A>G (p.Lys922=)
NM_000245.4(MET):c.2935C>T (p.His979Tyr) rs1584955347
NM_000245.4(MET):c.3208G>T (p.Val1070Leu) rs760285693
NM_000245.4(MET):c.3637G>A (p.Asp1213Asn)
NM_000245.4(MET):c.3688T>C (p.Tyr1230His) rs121913247
NM_000245.4(MET):c.3945A>T (p.Val1315=) rs879254340
NM_000245.4(MET):c.4118A>G (p.Asp1373Gly) rs773898036
NM_000245.4(MET):c.569A>G (p.Asp190Gly) rs1028165414
NM_000245.4(MET):c.638C>T (p.Ser213Leu)
NM_000245.4(MET):c.709G>A (p.Val237Ile) rs757402499
NM_000245.4(MET):c.818C>T (p.Thr273Ile)
NM_000245.4(MET):c.850A>G (p.Ile284Val) rs776014448
NM_000245.4(MET):c.934G>A (p.Glu312Lys)

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