Primary Site >> Stomach Cancer
Gene >> PTGR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309195 |
| Start | 111570174:111570174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376212074 |
| CDS Mutation | c.796C>T |
| AA Mutation | p.Arg266Cys(p.R266C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309195 |
| Start | 111586079:111586079(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.296G>C |
| AA Mutation | p.Gly99Ala(p.G99A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309195 |
| Start | 111597404:111597404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.19T>C |
| AA Mutation | p.Trp7Arg(p.W7R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309195 |
| Start | 111574772:111574772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.722C>T |
| AA Mutation | p.Ala241Val(p.A241V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309195 |
| Start | 111583543:111583543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.424G>A |
| AA Mutation | p.Gly142Arg(p.G142R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309195 |
| Start | 111563160:111563160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.951G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309195 |
| Start | 111563208:111563208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777442842 |
| CDS Mutation | c.903T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000309195 |
| Start | 111597322:111597322(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.101delA |
| AA Mutation | p.Asn34MetfsTer17(p.N34Mfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |