Primary Site >> Stomach Cancer
Gene >> PANX3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284288 |
| Start | 124619558:124619558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771739566 |
| CDS Mutation | c.802A>G |
| AA Mutation | p.Ile268Val(p.I268V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284288 |
| Start | 124613016:124613016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.218G>A |
| AA Mutation | p.Ser73Asn(p.S73N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284288 |
| Start | 124617457:124617457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372236130 |
| CDS Mutation | c.508G>A |
| AA Mutation | p.Asp170Asn(p.D170N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284288 |
| Start | 124617461:124617461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.512C>T |
| AA Mutation | p.Pro171Leu(p.P171L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284288 |
| Start | 124611614:124611614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751256451 |
| CDS Mutation | c.58C>T |
| AA Mutation | p.Arg20Cys(p.R20C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284288 |
| Start | 124611719:124611719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142639637 |
| CDS Mutation | c.163G>A |
| AA Mutation | p.Ala55Thr(p.A55T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |