Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

MET

MET proto-oncogene, receptor tyrosine kinase

Chromosome
7
Cytoband
7q31.2
Variants (rsID)
43

MET is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q31.2). Its official name is “MET proto-oncogene, receptor tyrosine kinase”. The reference table lists 43 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

21 reference-table entries with clinical significance.

  • rs11762213Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Renal cell carcinoma, papillary, 1|Renal cell carcinoma
  • rs33917957Benignsingle nucleotide variantRenal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Renal cell carcinoma
  • rs35225896Benignsingle nucleotide variantRenal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Renal cell carcinoma
  • rs35775721Benignsingle nucleotide variantHereditary cancer-predisposing syndrome|Renal cell carcinoma, papillary, 1|Renal cell carcinoma|Autosomal recessive nonsyndromic hearing loss 97
  • rs180985111Conflicting interpretationssingle nucleotide variantLymphedema|Hereditary cancer-predisposing syndrome|Renal cell carcinoma, papillary, 1|Renal cell carcinoma
  • rs200074800Conflicting interpretationssingle nucleotide variantRenal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Renal cell carcinoma|Hepatocellular carcinoma
  • rs200861145Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Renal cell carcinoma|Intellectual disability|Autosomal recessive nonsyndromic hearing loss 97
  • rs201315884Conflicting interpretationssingle nucleotide variantRenal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Renal cell carcinoma
  • rs201687037Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Renal cell carcinoma|Autosomal recessive nonsyndromic hearing loss 97
  • rs34589476Conflicting interpretationssingle nucleotide variantRenal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Neoplasm|Renal cell carcinoma|Hepatocellular carcinoma
  • rs45520237Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Renal cell carcinoma
  • rs45612435Conflicting interpretationssingle nucleotide variantRenal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Renal cell carcinoma
  • rs56391007Conflicting interpretationssingle nucleotide variantRenal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Congenital diaphragmatic hernia|Carcinoma|Neoplasm|Renal cell carcinoma|Classic Hodgkin lymphoma
  • rs786202191Conflicting interpretationssingle nucleotide variantHereditary cancer-predisposing syndrome|Renal cell carcinoma
  • rs587780738Likely benignsingle nucleotide variantRenal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Renal cell carcinoma
  • rs121913243Pathogenicsingle nucleotide variantRenal cell carcinoma, papillary, 1|Renal carcinoma|Renal cell carcinoma
  • rs121913670Pathogenicsingle nucleotide variantRenal cell carcinoma, papillary, 1|Hereditary cancer-predisposing syndrome|Renal cell carcinoma
  • rs786202724Pathogenicsingle nucleotide variantHereditary cancer-predisposing syndrome|Neoplasm|Carcinoma|Renal cell carcinoma, papillary, 1|Renal cell carcinoma
  • rs121913247Uncertain significancesingle nucleotide variantCarcinoma|Renal carcinoma
  • rs200690492Uncertain significancesingle nucleotide variantRenal cell carcinoma|Hereditary cancer-predisposing syndrome
  • rs764052874Uncertain significancesingle nucleotide variantHereditary cancer-predisposing syndrome|Renal cell carcinoma, papillary, 1|Renal cell carcinoma

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.