Primary Site >> Stomach Cancer
Gene >> ENTPD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371205 |
| Start | 95845443:95845443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.660A>C |
| AA Mutation | p.Gln220His(p.Q220H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371205 |
| Start | 95845477:95845477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.694T>A |
| AA Mutation | p.Ser232Thr(p.S232T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000453258 |
| Start | 95711966:95711966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10A>G |
| AA Mutation | p.Thr4Ala(p.T4A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371205 |
| Start | 95860569:95860569(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751221623 |
| CDS Mutation | c.1175A>G |
| AA Mutation | p.Gln392Arg(p.Q392R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371205 |
| Start | 95864761:95864761(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1226T>C |
| AA Mutation | p.Leu409Pro(p.L409P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371205 |
| Start | 95845502:95845502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375311388 |
| CDS Mutation | c.719G>A |
| AA Mutation | p.Arg240His(p.R240H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |