Primary Site >> Stomach Cancer
Gene >> TRIP10
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313244 |
| Start | 6746456:6746456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1157T>C |
| AA Mutation | p.Val386Ala(p.V386A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313244 |
| Start | 6743575:6743575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759899109 |
| CDS Mutation | c.490G>A |
| AA Mutation | p.Ala164Thr(p.A164T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313244 |
| Start | 6742982:6742982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.213G>T |
| AA Mutation | p.Gln71His(p.Q71H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313244 |
| Start | 6751153:6751153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1748G>A |
| AA Mutation | p.Arg583Gln(p.R583Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000313244 |
| Start | 6743519:6743519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.434G>A |
| AA Mutation | p.Cys145Tyr(p.C145Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000313244 |
| Start | 6743073:6743073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.304C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000313244 |
| Start | 6741235:6741235(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.156delA |
| AA Mutation | p.Lys52AsnfsTer29(p.K52Nfs*29) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000313244 |
| Start | 6744915:6744915(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.909delC |
| AA Mutation | p.Ser304ArgfsTer59(p.S304Rfs*59) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000313244 |
| Start | 6750369:6750369(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1479delC |
| AA Mutation | p.Ala494LeufsTer49(p.A494Lfs*49) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000313244 |
| Start | 6750368:6750369(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs762545513 |
| CDS Mutation | c.1479dupC |
| AA Mutation | p.Ala494ArgfsTer2(p.A494Rfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000313244 |
| Start | 6750598:6750615(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1626_1643delAGGTCACTGTGTGGCCAT |
| AA Mutation | p.Gly543_Ile548del(p.G543_I548del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |