Primary Site >> Stomach Cancer
Gene >> ACP5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218758 |
| Start | 11576269:11576269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.709C>A |
| AA Mutation | p.Leu237Met(p.L237M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218758 |
| Start | 11576284:11576284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374180791 |
| CDS Mutation | c.694G>A |
| AA Mutation | p.Gly232Arg(p.G232R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218758 |
| Start | 11576451:11576451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774878498 |
| CDS Mutation | c.527G>A |
| AA Mutation | p.Arg176Gln(p.R176Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218758 |
| Start | 11577253:11577253(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.65C>T |
| AA Mutation | p.Ala22Val(p.A22V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218758 |
| Start | 11575186:11575186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.802A>C |
| AA Mutation | p.Lys268Gln(p.K268Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218758 |
| Start | 11576433:11576433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778805198 |
| CDS Mutation | c.545G>A |
| AA Mutation | p.Arg182His(p.R182H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218758 |
| Start | 11576447:11576447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369197756 |
| CDS Mutation | c.531C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218758 |
| Start | 11577069:11577069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.249C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218758 |
| Start | 11575232:11575232(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139096747 |
| CDS Mutation | c.756C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |