Primary Site >> Stomach Cancer
Gene >> PODXL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378555 |
| Start | 131506635:131506635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201911803 |
| CDS Mutation | c.1193G>A |
| AA Mutation | p.Arg398Gln(p.R398Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378555 |
| Start | 131511175:131511175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.359T>A |
| AA Mutation | p.Ile120Asn(p.I120N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378555 |
| Start | 131511394:131511394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375173959 |
| CDS Mutation | c.140C>T |
| AA Mutation | p.Pro47Leu(p.P47L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378555 |
| Start | 131511053:131511053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.481A>G |
| AA Mutation | p.Lys161Glu(p.K161E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378555 |
| Start | 131504419:131504419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1569G>T |
| AA Mutation | p.Gln523His(p.Q523H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378555 |
| Start | 131510965:131510965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201501253 |
| CDS Mutation | c.569G>A |
| AA Mutation | p.Arg190Gln(p.R190Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378555 |
| Start | 131509551:131509551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.837C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378555 |
| Start | 131506719:131506719(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1109delG |
| AA Mutation | p.Gly370AlafsTer7(p.G370Afs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |