Primary Site >> Stomach Cancer
Gene >> TOX
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361421 |
| Start | 58959981:58959981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.130A>C |
| AA Mutation | p.Met44Leu(p.M44L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361421 |
| Start | 58826875:58826875(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.952A>G |
| AA Mutation | p.Lys318Glu(p.K318E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361421 |
| Start | 58838173:58838173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776756583 |
| CDS Mutation | c.832G>A |
| AA Mutation | p.Ala278Thr(p.A278T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361421 |
| Start | 58838267:58838267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.738A>C |
| AA Mutation | p.Lys246Asn(p.K246N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361421 |
| Start | 58851624:58851624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.593G>T |
| AA Mutation | p.Ser198Ile(p.S198I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361421 |
| Start | 58838266:58838266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201277886 |
| CDS Mutation | c.739C>A |
| AA Mutation | p.Pro247Thr(p.P247T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361421 |
| Start | 58838187:58838187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.818G>A |
| AA Mutation | p.Arg273His(p.R273H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361421 |
| Start | 58939438:58939438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.275G>A |
| AA Mutation | p.Gly92Asp(p.G92D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361421 |
| Start | 58815456:58815456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201330163 |
| CDS Mutation | c.1274C>T |
| AA Mutation | p.Pro425Leu(p.P425L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361421 |
| Start | 58838105:58838105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs62640919 |
| CDS Mutation | c.900C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361421 |
| Start | 58838198:58838198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376393252 |
| CDS Mutation | c.807G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361421 |
| Start | 58851737:58851737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.480A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361421 |
| Start | 58838174:58838174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549813687 |
| CDS Mutation | c.831C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361421 |
| Start | 58815488:58815488(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1242T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361421 |
| Start | 58815668:58815668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201668109 |
| CDS Mutation | c.1062G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361421 |
| Start | 58838218:58838228(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.777_787delTGAGCCCCAGA |
| AA Mutation | p.Asn259LysfsTer12(p.N259Kfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000361421 |
| Start | 58815376:58815376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1354C>T |
| AA Mutation | p.Gln452Ter(p.Q452*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361421 |
| Start | 58838266:58838267(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.738dupA |
| AA Mutation | p.Pro247ThrfsTer14(p.P247Tfs*14) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000361421 |
| Start | 58851806:58851806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.412-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |