Primary Site >> Stomach Cancer
Gene >> GIT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225394 |
| Start | 29576116:29576116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1627G>A |
| AA Mutation | p.Ala543Thr(p.A543T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225394 |
| Start | 29574755:29574755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2233G>A |
| AA Mutation | p.Ala745Thr(p.A745T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225394 |
| Start | 29576637:29576637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376860718 |
| CDS Mutation | c.1265C>T |
| AA Mutation | p.Thr422Met(p.T422M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000225394 |
| Start | 29576367:29576367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144848199 |
| CDS Mutation | c.1464G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000225394 |
| Start | 29576617:29576617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751546077 |
| CDS Mutation | c.1285C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000225394 |
| Start | 29576935:29576935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1155C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000225394 |
| Start | 29578327:29578327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368894186 |
| CDS Mutation | c.855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |