Primary Site >> Stomach Cancer
Gene >> PBX3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373489 |
| Start | 125963024:125963024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778017986 |
| CDS Mutation | c.1135C>T |
| AA Mutation | p.Arg379Cys(p.R379C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373489 |
| Start | 125963037:125963037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1148A>G |
| AA Mutation | p.Asn383Ser(p.N383S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373489 |
| Start | 125929842:125929842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.704C>T |
| AA Mutation | p.Ala235Val(p.A235V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373489 |
| Start | 125963082:125963082(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1193A>G |
| AA Mutation | p.Tyr398Cys(p.Y398C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373489 |
| Start | 125915861:125915861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.450A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373489 |
| Start | 125960791:125960791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368535684 |
| CDS Mutation | c.951C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000373489 |
| Start | 125965877:125965879(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773571000 |
| CDS Mutation | c.1261_1263delCCT |
| AA Mutation | p.Pro421del(p.P421del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |