Table 2

Clinicopathological characteristics and genotype of the RHOA mutant gastric cancers

Case numberGenderAge at diagnosisTumour localisationLaurén phenotypeT-categoryN-categoryM-categoryUICC stageTumour gradeKRAS codon 12 and 13PIK3CA exon 9PIK3CA exon 20MSI statusEBV statusHelicobacter pylori statusRHOA mutationRHOA exonRHOA substitution mutationFunctional region—interaction with
1F44DistalDiffuseT1bN0M0IAG2WTWTWTMSSmvc.125A>G, p.Y42C2TransitionEffector domain
2F38DistalDiffuseT3N1M0IIIAG3WTWTWTMSSc.169T>G, p.L57V3TransversionPKN/PRK1
3F66DistalDiffuseT1aN0M0IAG3WTWTWTMSSc.169T>G, p.L57V3TransversionPKN/PRK1
4F80DistalDiffuseT4aN2M0IIIBG3WTWTWTMSSc.65_66delinsGT, p.L22R2Deletion/Insertion
5F68DistalDiffuseT4aN3aM0IIICG3WTWTWTMSSmvc.206T>G, p.L69R#3Transversion
6F69ProximalDiffuseT2N0M0IBG3WTWTWTMSSc.125A>G, p.Y42C2TransitionEffector domain
7M90ProximalDiffuseT3N3M0IIIBG3WTWTWTMSSc.50G>A, p.G17E2TransitionGTP
8M68ProximalDiffuseT3N2M0IIIAG3WTWTWTMSSc.14G>A, p.R5Q2Transition
9M62DistalDiffuseT3N2M0IIIAG3WTWTWTMSSmvc.109A>G, p.T37A#2TransitionEffector domain
10F72DistalIntestinalT3N3aM0IIIBG3WTWTWTMSSc.125A>G, p.Y42C2TransitionEffector domain
11M84DistalIntestinalT2N0M0IBG3WTWTWTMSSc.125A>G, p.Y42C2TransitionEffector domain
12M85DistalIntestinalT2N3aM0IIIAG3WTWTWTMSSc.70G>T, p.V24F2Transversion
13M66DistalIntestinalT3N0M0IIAG3WTWTWTMSI+c.50delinsAA, p.G17Efs*24#2Deletion/InsertionGTP
14F80DistalUnclassifiedT3N1M0IIBG3WTWTWTMSSc.169T>G, p.L57V3TransversionPKN/PRK1
15F58DistalUnclassifiedT1bN3bM0IIBG3WTWTWTMSSc.125A>G, p.Y42C2TransitionEffector domain
16M59DistalMixedT4bN3aM0IIICG3WTMUTWTMSS++c.14G>A, p.R5Q2Transition
  • #, hitherto unreported mutations; −, negative; +, positive; EBV, Epstein–Barr virus; GTP, guanosine triphosphate; MSI, microsatellite instable; MSS, microsatellite stable; mv, missing value; PKN/PRK1, protein kinase N1; UICC, Union for International Cancer Control; WT, wildtype.