Primary Site >> Stomach Cancer
Gene >> AGT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366667 |
| Start | 230703224:230703224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1375C>G |
| AA Mutation | p.Pro459Ala(p.P459A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366667 |
| Start | 230710600:230710600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61762540 |
| CDS Mutation | c.251T>C |
| AA Mutation | p.Leu84Pro(p.L84P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366667 |
| Start | 230710220:230710220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs567719599 |
| CDS Mutation | c.631G>A |
| AA Mutation | p.Val211Met(p.V211M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366667 |
| Start | 230703270:230703270(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1329C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366667 |
| Start | 230710473:230710473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143232180 |
| CDS Mutation | c.378C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366667 |
| Start | 230710056:230710056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.795C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000366667 |
| Start | 230703309:230703309(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs387906578 |
| CDS Mutation | c.1290delT |
| AA Mutation | p.Phe430LeufsTer25(p.F430Lfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |