Primary Site >> Stomach Cancer
Gene >> KRAS
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25245347:25245347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112445441 |
| CDS Mutation | c.38G>A |
| AA Mutation | p.Gly13Asp(p.G13D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25227349:25227349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913528 |
| CDS Mutation | c.175G>A |
| AA Mutation | p.Ala59Thr(p.A59T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| 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 | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256078 |
| Start | 25225628:25225628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121913527 |
| CDS Mutation | c.436G>A |
| AA Mutation | p.Ala146Thr(p.A146T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000256078 |
| Start | 25215559:25215559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.452G>C |
| AA Mutation | p.Arg151Thr(p.R151T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| 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 |
| ID | 7 |
| 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 | 8 |
| 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 | 9 |
| 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 |