Primary Site >> Liver Cancer
Gene >> P2RY1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836634:152836634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.852G>C |
| AA Mutation | p.Leu284Phe(p.L284F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836089:152836089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.307A>C |
| AA Mutation | p.Thr103Pro(p.T103P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836533:152836533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751A>T |
| AA Mutation | p.Asn251Tyr(p.N251Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152835904:152835904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766253716 |
| CDS Mutation | c.122A>T |
| AA Mutation | p.Lys41Ile(p.K41I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305097 |
| Start | 152836531:152836531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768092598 |
| CDS Mutation | c.749A>T |
| AA Mutation | p.Asp250Val(p.D250V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| 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 |