Research Article
RNF43 Mutations in IPMN Cases: A Potential Prognostic Factor
Table 4
Mutations of KRAS/GNAS/RNF43 identified in IPMN.
| Gene | Mutation | Amino acid | |
| KRAS | c.34G>C | p.G12R | 2 | c.34G>T | p.G12C | 2 | c.35G>A | p.G12D | 12 | c.35G>T | p.G12V | 11 | c.34G>A/35G>A | p.G12N | 1 | c.38G>A | p.G13D | 2 | c.182A>G | p.Q61R | 5 |
| GNAS | c.601C>T | p.R201C | 22 | c.602G>A | p.R201H | 17 | c.601C>T/c.602G>A | p.R201Y | 1 |
| RNF43 | NM_017763:exon8:c.879delG | p.E293fs | 1 | NM_017763:exon7:c.700C>T | p.Q234X | 1 | NM_017763:exon7:c.689delA | p.D230fs | 1 | NM_017763:exon4:c.253-2A>T | | 1 | NM_017763:exon9:c.952+15A>G | | 1 | NM_017763:exon9:c.1093G>A | p.A365T | 3 |
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