Primary Site >> Stomach Cancer
Gene >> GTSE1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454366 |
| Start | 46323220:46323220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1463T>G |
| AA Mutation | p.Leu488Arg(p.L488R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454366 |
| Start | 46328761:46328761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1798C>T |
| AA Mutation | p.Pro600Ser(p.P600S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000454366 |
| Start | 46308936:46308936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.755C>G |
| AA Mutation | p.Ala252Gly(p.A252G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000454366 |
| Start | 46312251:46312251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150217285 |
| CDS Mutation | c.873G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000454366 |
| Start | 46316318:46316318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757579901 |
| CDS Mutation | c.1338T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000454366 |
| Start | 46329441:46329441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2010C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000454366 |
| Start | 46308568:46308568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.387T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000454366 |
| Start | 46316334:46316334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780615307 |
| CDS Mutation | c.1354C>T |
| AA Mutation | p.Arg452Ter(p.R452*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |