PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 21253810-1 2011 The most important mutation associated with Multiple Endocrine Neoplasia type 2B (MEN 2B) is the change of thymine to cytosine in codon 918 of exon 16 in the RET oncogene (ATG ACG). Thymine 107-114 ret proto-oncogene Homo sapiens 44-80 21253810-1 2011 The most important mutation associated with Multiple Endocrine Neoplasia type 2B (MEN 2B) is the change of thymine to cytosine in codon 918 of exon 16 in the RET oncogene (ATG ACG). Thymine 107-114 ret proto-oncogene Homo sapiens 82-88 21253810-1 2011 The most important mutation associated with Multiple Endocrine Neoplasia type 2B (MEN 2B) is the change of thymine to cytosine in codon 918 of exon 16 in the RET oncogene (ATG ACG). Thymine 107-114 ret proto-oncogene Homo sapiens 158-161 9012117-3 1996 The most frequent hereditary mutation found in MEN 2A and FMTC groups is substitution of thymine for cytosine in position 2095 of the transmembranous domain of the Ret-tyrosine kinase gene. Thymine 89-96 ret proto-oncogene Homo sapiens 47-53 9012117-3 1996 The most frequent hereditary mutation found in MEN 2A and FMTC groups is substitution of thymine for cytosine in position 2095 of the transmembranous domain of the Ret-tyrosine kinase gene. Thymine 89-96 ret proto-oncogene Homo sapiens 164-167 23660265-7 2013 Gene analysis confirmed heterozygous mis-sense mutation at codon 918 in exon 16 of RET proto-oncogene in which thymine was replaced by cytosine (ATG ACG). Thymine 111-118 ret proto-oncogene Homo sapiens 83-86