Primary Site >> Stomach Cancer
Gene >> TAPBP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426633 |
| Start | 33305045:33305045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812C>T |
| AA Mutation | p.Ala271Val(p.A271V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426633 |
| Start | 33313321:33313321(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.365C>A |
| AA Mutation | p.Ala122Asp(p.A122D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426633 |
| Start | 33313759:33313759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.143G>A |
| AA Mutation | p.Arg48His(p.R48H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426633 |
| Start | 33304566:33304566(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941T>G |
| AA Mutation | p.Leu314Arg(p.L314R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426633 |
| Start | 33304501:33304501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1006C>A |
| AA Mutation | p.Pro336Thr(p.P336T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000426633 |
| Start | 33305283:33305283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146216992 |
| CDS Mutation | c.574G>A |
| AA Mutation | p.Ala192Thr(p.A192T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000426633 |
| Start | 33313350:33313350(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.336G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000426633 |
| Start | 33313827:33313827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.75C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000426633 |
| Start | 33313443:33313443(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.243G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000426633 |
| Start | 33305296:33305296(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.561delC |
| AA Mutation | p.Thr188ProfsTer17(p.T188Pfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000426633 |
| Start | 33304494:33304494(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1013delG |
| AA Mutation | p.Gly338AlafsTer65(p.G338Afs*65) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000426633 |
| Start | 33304398:33304398(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1109delC |
| AA Mutation | p.Pro370GlnfsTer33(p.P370Qfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000426633 |
| Start | 33304600:33304600(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.907delC |
| AA Mutation | p.Arg303GlyfsTer100(p.R303Gfs*100) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000426633 |
| Start | 33305073:33305073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764303150 |
| CDS Mutation | c.784C>T |
| AA Mutation | p.Gln262Ter(p.Q262*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000426633 |
| Start | 33314035:33314037(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5_7delAGT |
| AA Mutation | p.Lys2_Ser3delinsThr(p.K2_S3delinsT) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |