List of variants in gene MET reported as likely benign 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: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
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.632T>G (p.Leu211Trp)	rs45483396	0.00005
NM_000245.4(MET):c.1881T>C (p.Gly627=)	rs200050499	0.00004
NM_000245.4(MET):c.3945A>T (p.Val1315=)	rs879254340

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