Primary Site >> Stomach Cancer
Gene >> PAK4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358301 |
| Start | 39173991:39173991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777017835 |
| CDS Mutation | c.1079G>A |
| AA Mutation | p.Arg360His(p.R360H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358301 |
| Start | 39176663:39176663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1433C>T |
| AA Mutation | p.Thr478Met(p.T478M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358301 |
| Start | 39176677:39176677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780795083 |
| CDS Mutation | c.1447G>A |
| AA Mutation | p.Ala483Thr(p.A483T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358301 |
| Start | 39176680:39176680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1450C>T |
| AA Mutation | p.Pro484Ser(p.P484S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358301 |
| Start | 39178533:39178533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762977178 |
| CDS Mutation | c.1730C>T |
| AA Mutation | p.Pro577Leu(p.P577L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000358301 |
| Start | 39178569:39178569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1766G>A |
| AA Mutation | p.Arg589His(p.R589H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000358301 |
| Start | 39176703:39176703(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1473C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000358301 |
| Start | 39177725:39177726(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs769136911 |
| CDS Mutation | c.1542dupC |
| AA Mutation | p.Tyr515LeufsTer124(p.Y515Lfs*124) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |