Primary Site >> Stomach Cancer
Gene >> TROAP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257909 |
| Start | 49329444:49329444(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1154C>T |
| AA Mutation | p.Ala385Val(p.A385V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257909 |
| Start | 49330383:49330383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1538A>G |
| AA Mutation | p.Gln513Arg(p.Q513R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257909 |
| Start | 49330220:49330220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1375G>A |
| AA Mutation | p.Gly459Arg(p.G459R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257909 |
| Start | 49330395:49330395(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201922610 |
| CDS Mutation | c.1550C>T |
| AA Mutation | p.Pro517Leu(p.P517L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257909 |
| Start | 49325850:49325850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.599G>A |
| AA Mutation | p.Gly200Asp(p.G200D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257909 |
| Start | 49329179:49329179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749320809 |
| CDS Mutation | c.1039C>T |
| AA Mutation | p.Arg347Trp(p.R347W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000257909 |
| Start | 49327235:49327235(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201119814 |
| CDS Mutation | c.796G>A |
| AA Mutation | p.Glu266Lys(p.E266K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257909 |
| Start | 49325559:49325559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.396A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000257909 |
| Start | 49329208:49329208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1068G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257909 |
| Start | 49330900:49330900(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs753006677 |
| CDS Mutation | c.2055delT |
| AA Mutation | p.Ile686SerfsTer7(p.I686Sfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257909 |
| Start | 49324022:49324022(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.326delC |
| AA Mutation | p.Pro109LeufsTer10(p.P109Lfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000257909 |
| Start | 49325846:49325846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.595C>T |
| AA Mutation | p.Arg199Ter(p.R199*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000257909 |
| Start | 49331597:49331598(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2323dupC |
| AA Mutation | p.Gln775ProfsTer19(p.Q775Pfs*19) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |