Primary Site >> Stomach Cancer
Gene >> LIMS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355119 |
| Start | 127643028:127643028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.404T>C |
| AA Mutation | p.Leu135Pro(p.L135P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355119 |
| Start | 127642126:127642126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560750824 |
| CDS Mutation | c.583G>A |
| AA Mutation | p.Val195Ile(p.V195I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355119 |
| Start | 127654878:127654878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.190T>G |
| AA Mutation | p.Cys64Gly(p.C64G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355119 |
| Start | 127642075:127642075(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762554883 |
| CDS Mutation | c.634G>A |
| AA Mutation | p.Ala212Thr(p.A212T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355119 |
| Start | 127640926:127640926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.723C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355119 |
| Start | 127654846:127654846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.222G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355119 |
| Start | 127642076:127642076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766044187 |
| CDS Mutation | c.633C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |