Primary Site >> Stomach Cancer
Gene >> TRIM24
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343526 |
| Start | 138551072:138551072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755272421 |
| CDS Mutation | c.1153C>T |
| AA Mutation | p.Arg385Trp(p.R385W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343526 |
| Start | 138584935:138584935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs560006714 |
| CDS Mutation | c.3137G>A |
| AA Mutation | p.Arg1046His(p.R1046H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343526 |
| Start | 138538676:138538676(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772873132 |
| CDS Mutation | c.1016G>A |
| AA Mutation | p.Arg339His(p.R339H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343526 |
| Start | 138567626:138567626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756911125 |
| CDS Mutation | c.1676C>T |
| AA Mutation | p.Ala559Val(p.A559V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343526 |
| Start | 138580629:138580629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2653C>T |
| AA Mutation | p.Pro885Ser(p.P885S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343526 |
| Start | 138570900:138570900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377565012 |
| CDS Mutation | c.1775C>T |
| AA Mutation | p.Thr592Met(p.T592M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000343526 |
| Start | 138584793:138584793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554322561 |
| CDS Mutation | c.2995G>A |
| AA Mutation | p.Glu999Lys(p.E999K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343526 |
| Start | 138554936:138554936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1500G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000343526 |
| Start | 138525295:138525295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780633491 |
| CDS Mutation | c.819A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |