Primary Site >> Stomach Cancer
Gene >> TOX3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219746 |
| Start | 52439806:52439806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754057654 |
| CDS Mutation | c.1150G>A |
| AA Mutation | p.Ala384Thr(p.A384T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219746 |
| Start | 52468537:52468537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568437917 |
| CDS Mutation | c.125C>T |
| AA Mutation | p.Ala42Val(p.A42V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219746 |
| Start | 52439285:52439285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773476008 |
| CDS Mutation | c.1671C>G |
| AA Mutation | p.His557Gln(p.H557Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219746 |
| Start | 52450406:52450406(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201685761 |
| CDS Mutation | c.549C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219746 |
| Start | 52439819:52439819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566980343 |
| CDS Mutation | c.1137C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000219746 |
| Start | 52464019:52464019(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.323delC |
| AA Mutation | p.Pro108LeufsTer45(p.P108Lfs*45) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000219746 |
| Start | 52444324:52444324(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.939delA |
| AA Mutation | p.Glu314AsnfsTer3(p.E314Nfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000219746 |
| Start | 52445996:52445996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.904C>T |
| AA Mutation | p.Gln302Ter(p.Q302*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000219746 |
| Start | 52439883:52439885(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1071_1073delTCT |
| AA Mutation | p.Leu358del(p.L358del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000219746 |
| Start | 52439430:52439489(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1467_1526delCCTGCAGCAGCAGCAGCAGCATCTCCAGCAGCAAATTAATCAACAGCAGCTGCAGCAGCA |
| AA Mutation | p.His489_Gln508del(p.H489_Q508del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |