Primary Site >> Stomach Cancer
Gene >> TBXA2R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600564:3600564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.71T>C |
| AA Mutation | p.Leu24Pro(p.L24P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600162:3600162(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.473C>T |
| AA Mutation | p.Ala158Val(p.A158V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375190 |
| Start | 3595743:3595743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745986396 |
| CDS Mutation | c.977G>A |
| AA Mutation | p.Arg326Gln(p.R326Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600598:3600598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.37C>T |
| AA Mutation | p.Arg13Trp(p.R13W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600478:3600478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201236133 |
| CDS Mutation | c.157C>T |
| AA Mutation | p.Arg53Trp(p.R53W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600346:3600346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.289G>A |
| AA Mutation | p.Ala97Thr(p.A97T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600262:3600262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.373G>A |
| AA Mutation | p.Ala125Thr(p.A125T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600237:3600237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.398G>A |
| AA Mutation | p.Gly133Asp(p.G133D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600071:3600071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199672500 |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600356:3600356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.279C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600464:3600464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752519324 |
| CDS Mutation | c.171G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600329:3600329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.306C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600155:3600155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.480G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375190 |
| Start | 3595835:3595835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.885C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375190 |
| Start | 3600365:3600365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568910789 |
| CDS Mutation | c.270C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |