Primary Site >> Stomach Cancer
Gene >> TGFBRAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105267433:105267433(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139792932 |
| CDS Mutation | c.2533G>A |
| AA Mutation | p.Ala845Thr(p.A845T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105296403:105296403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.991G>A |
| AA Mutation | p.Val331Ile(p.V331I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105298604:105298604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.790G>A |
| AA Mutation | p.Asp264Asn(p.D264N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000258449 |
| Start | 105273689:105273689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1667T>C |
| AA Mutation | p.Val556Ala(p.V556A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105307781:105307781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.521C>A |
| AA Mutation | p.Ala174Asp(p.A174D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105269450:105269450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755371712 |
| CDS Mutation | c.2228G>A |
| AA Mutation | p.Arg743His(p.R743H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105298673:105298673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368179993 |
| CDS Mutation | c.721C>T |
| AA Mutation | p.Arg241Cys(p.R241C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258449 |
| Start | 105308109:105308109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.193G>A |
| AA Mutation | p.Ala65Thr(p.A65T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258449 |
| Start | 105298650:105298650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.744G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258449 |
| Start | 105308278:105308278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766664518 |
| CDS Mutation | c.24G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258449 |
| Start | 105269593:105269593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs565390607 |
| CDS Mutation | c.2085G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258449 |
| Start | 105308203:105308203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.99C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258449 |
| Start | 105284333:105284333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1104A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258449 |
| Start | 105307927:105307927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746399074 |
| CDS Mutation | c.375C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000258449 |
| Start | 105307947:105307947(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.355delG |
| AA Mutation | p.Ala119GlnfsTer6(p.A119Qfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000258449 |
| Start | 105269325:105269325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2353C>T |
| AA Mutation | p.Gln785Ter(p.Q785*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000258449 |
| Start | 105284335:105284335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1102G>T |
| AA Mutation | p.Glu368Ter(p.E368*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant;splice_region_variant |
| Transcription ID | ENST00000258449 |
| Start | 105298703:105298704(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.690dupC |
| AA Mutation | p.Met231HisfsTer35(p.M231Hfs*35) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |