Primary Site >> Stomach Cancer
Gene >> HTR1E
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305344 |
| Start | 87015386:87015386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.52A>G |
| AA Mutation | p.Thr18Ala(p.T18A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305344 |
| Start | 87015863:87015863(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.529C>T |
| AA Mutation | p.His177Tyr(p.H177Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305344 |
| Start | 87015840:87015840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775040501 |
| CDS Mutation | c.506C>T |
| AA Mutation | p.Pro169Leu(p.P169L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305344 |
| Start | 87015770:87015770(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200719637 |
| CDS Mutation | c.436G>A |
| AA Mutation | p.Val146Ile(p.V146I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305344 |
| Start | 87015611:87015611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.277T>C |
| AA Mutation | p.Phe93Leu(p.F93L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000305344 |
| Start | 87016111:87016111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.777C>A |
| AA Mutation | p.Phe259Leu(p.F259L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305344 |
| Start | 87016429:87016429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1095T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305344 |
| Start | 87015955:87015955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377350581 |
| CDS Mutation | c.621C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305344 |
| Start | 87016198:87016198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.864G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000305344 |
| Start | 87015904:87015904(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140545385 |
| CDS Mutation | c.570G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |