Primary Site >> Stomach Cancer
Gene >> AP5B1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000532090 |
| Start | 65778331:65778331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2162C>T |
| AA Mutation | p.Ala721Val(p.A721V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000532090 |
| Start | 65778694:65778694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369106728 |
| CDS Mutation | c.1799C>T |
| AA Mutation | p.Ala600Val(p.A600V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000532090 |
| Start | 65778055:65778055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2438G>A |
| AA Mutation | p.Arg813His(p.R813H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000532090 |
| Start | 65779262:65779262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1231G>A |
| AA Mutation | p.Ala411Thr(p.A411T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000532090 |
| Start | 65778367:65778367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2126C>T |
| AA Mutation | p.Ala709Val(p.A709V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000532090 |
| Start | 65779921:65779921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.572T>C |
| AA Mutation | p.Leu191Pro(p.L191P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000532090 |
| Start | 65778899:65778899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1594G>T |
| AA Mutation | p.Gly532Cys(p.G532C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000532090 |
| Start | 65779148:65779148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368800811 |
| CDS Mutation | c.1345C>T |
| AA Mutation | p.Arg449Trp(p.R449W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000532090 |
| Start | 65778855:65778855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1638G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000532090 |
| Start | 65778900:65778900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758507175 |
| CDS Mutation | c.1593G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |