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. 2019 Oct 18;9:1088. doi: 10.3389/fonc.2019.01088

Table 1.

Most common mutations in the individual codons of RAS proteins.

RAS protein Malignancies Codon Amino acid substitution
HRAS Dermatological
Head and neck cancer
Codon 12: GGC (Gly, G) 12A, 12C, 12D, 12R, 12S, 12V
Codon 13: GGT (Gly, G) 13C, 13D, 13R, 13S, 13V
Codon 61: CAG (Gln, Q) 61H, 61K, 61L, 61P, 61R
KRAS Pancreatic carcinoma
Colorectal cancer
Lung malignancies
Codon 12: GGT (Gly, G) 12A, 12C, 12D, 12R, 12S, 12V
Codon 13: GGC (Gly, G) 13A, 13C, 13D, 13R, 13S, 13V
Codon 61: CAA (Gln, Q) 61E, 61H, 61K, 61L, 61P, 61R
NRAS Melanomas
Hematopoietic malignancies
Codon 12: GGT(Gly, G) 12A, 12C, 12D, 12R, 12S, 12V
Codon 13: GGT (Gly, G) 13A, 13C, 13D, 13R, 13S, 13V
Codon 61: CAA (Gln, Q) 61E, 61H, 61K, 61L, 61P, 61R

Amino acid substitutions identified at codon 12, 13, and 61 of each RAS protein, highlighting in red the most frequently observed. Gly and G, glycine; Gln and Q, glutamine; A, alanine; C, cysteine; D, aspartic acid; R, arginine; S, serine; V, valine; H, histidine; K, lysine; L, Leucine; P, proline; E, glutamic acid.