Primary Site >> Stomach Cancer
Gene >> P2RY1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836285:152836285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.503C>T |
| AA Mutation | p.Ala168Val(p.A168V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836366:152836366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.584G>A |
| AA Mutation | p.Arg195His(p.R195H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836195:152836195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.413G>A |
| AA Mutation | p.Ser138Asn(p.S138N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836696:152836696(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.914C>G |
| AA Mutation | p.Thr305Arg(p.T305R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836266:152836266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.484C>T |
| AA Mutation | p.Arg162Trp(p.R162W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305097 |
| Start | 152835872:152835872(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.90C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305097 |
| Start | 152835851:152835851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.69G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836682:152836682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.900C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836493:152836493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748490359 |
| CDS Mutation | c.711C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |