List of variants reported as uncertain significance 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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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
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.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.1640G>A (p.Arg547Gln)	rs761951444	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.3403A>T (p.Ser1135Cys)	rs1394199299	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.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.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

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