Primary Site >> Stomach Cancer
Gene >> PBX2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375050 |
| Start | 32186614:32186614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1190G>A |
| AA Mutation | p.Arg397Gln(p.R397Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375050 |
| Start | 32189821:32189821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.95C>T |
| AA Mutation | p.Pro32Leu(p.P32L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375050 |
| Start | 32188306:32188306(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.494T>G |
| AA Mutation | p.Leu165Arg(p.L165R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375050 |
| Start | 32187720:32187720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.797A>G |
| AA Mutation | p.His266Arg(p.H266R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375050 |
| Start | 32187263:32187263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1003C>A |
| AA Mutation | p.Pro335Thr(p.P335T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375050 |
| Start | 32188441:32188441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776784396 |
| CDS Mutation | c.359A>G |
| AA Mutation | p.Asn120Ser(p.N120S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375050 |
| Start | 32188429:32188429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.371C>T |
| AA Mutation | p.Ala124Val(p.A124V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375050 |
| Start | 32188298:32188298(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.502delA |
| AA Mutation | p.Ile168SerfsTer24(p.I168Sfs*24) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375050 |
| Start | 32189866:32189866(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773143486 |
| CDS Mutation | c.50delG |
| AA Mutation | p.Gly17AlafsTer5(p.G17Afs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |