Primary Site >> Stomach Cancer
Gene >> PIP4K2B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619039 |
| Start | 38771076:38771076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1004G>A |
| AA Mutation | p.Arg335Gln(p.R335Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619039 |
| Start | 38771038:38771038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1042G>A |
| AA Mutation | p.Val348Ile(p.V348I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000619039 |
| Start | 38770491:38770491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543549858 |
| CDS Mutation | c.1115C>T |
| AA Mutation | p.Thr372Met(p.T372M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619039 |
| Start | 38784285:38784285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.312A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000619039 |
| Start | 38778349:38778349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200521282 |
| CDS Mutation | c.678G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000619039 |
| Start | 38799277:38799277(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.148delG |
| AA Mutation | p.Val50Ter(p.V50*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000619039 |
| Start | 38778374:38778374(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.655-2A>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |