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Updated: Mar 30, 2026

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
Variability in penetrance of multiple endocrine neoplasia 2A with amino acid substitutions in RET codon 634
Andreas Machens1, Henning Dralle1
1Department of General, Visceral and Vascular Surgery, Martin-Luther-University Halle-Wittenberg, Halle (Saale), Germany.
Objective:
Controversy surrounds the importance of the different amino acids substituting for cysteine in REarranged during Transfection (RET) codon 634 for multiple endocrine neoplasia 2A (MEN 2A). This study aimed to clarify the relevance of these amino acid substitutions for the development of MEN 2A.
Design:
Cross-sectional study at surgical referral centres in Germany.
Patients:
Included were 184 carriers of RET mutations in codon 634.
Measurements:
Arginine (79 carriers) and tyrosine (50 carriers) substitutions in codon 634 were compared with each other and, for the first time, gauged against a common reference standard comprising all other amino acid substitutions (phenylalanine, 35 carriers; serine, 12 carriers; glycine, 7 carriers; tryptophan, 1 carrier).
Results:
Arginine substitutions in codon 634 were associated with higher penetrance of medullary thyroid cancer (MTC; 82% vs 62%; P = 0·010), any phaeochromocytoma (44% vs 15%, P < 0·001), bilateral phaeochromocytoma (32% vs 5%; P < 0·001) and primary hyperparathyroidism (18% vs 5%; P = 0·039) relative to the reference standard. The penetrance rates of any phaeochromocytoma (44% vs 26%; P = 0·041) and bilateral phaeochromocytoma (32% vs 14%; P = 0·035) were also higher with arginine than with tyrosine substitutions. Corrected for multiple testing, the associations of arginine with any phaeochromocytoma and bilateral phaeochromocytoma remained statistically significant. Progression of MTC, evidenced by largest primary tumour diameter, nodal status, distant metastasis and biochemical cure, did not differ by amino acid substitution.
Conclusions:
In codon 634, arginine substitutions for cysteine may cause slightly higher penetrance rates of MEN 2A which, overall, are too small to treat carriers differently. The mode of action by which arginine exerts these subtle effects warrants further research.
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