Primary Site >> Pancreatic Cancer
Gene >> KRAS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25245350:25245350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913529 |
| CDS Mutation | c.35G>A |
| AA Mutation | p.Gly12Asp(p.G12D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25245350:25245350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913529 |
| CDS Mutation | c.35G>T |
| AA Mutation | p.Gly12Val(p.G12V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25245351:25245351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913530 |
| CDS Mutation | c.34G>C |
| AA Mutation | p.Gly12Arg(p.G12R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25227342:25227342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913240 |
| CDS Mutation | c.182A>G |
| AA Mutation | p.Gln61Arg(p.Q61R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25245351:25245351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913530 |
| CDS Mutation | c.34G>T |
| AA Mutation | p.Gly12Cys(p.G12C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25227341:25227341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs17851045 |
| CDS Mutation | c.183A>C |
| AA Mutation | p.Gln61His(p.Q61H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25245348:25245348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913535 |
| CDS Mutation | c.37G>T |
| AA Mutation | p.Gly13Cys(p.G13C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25245350:25245350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913529 |
| CDS Mutation | c.35G>C |
| AA Mutation | p.Gly12Ala(p.G12A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25227341:25227341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs17851045 |
| CDS Mutation | c.183A>T |
| AA Mutation | p.Gln61His(p.Q61H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25245351:25245351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913530 |
| CDS Mutation | c.34G>A |
| AA Mutation | p.Gly12Ser(p.G12S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |