Primary Site >> Stomach Cancer
Gene >> SOX3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504564:140504564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.497A>C |
| AA Mutation | p.Asn166Thr(p.N166T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504475:140504475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.586C>T |
| AA Mutation | p.Arg196Cys(p.R196C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504474:140504474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.587G>A |
| AA Mutation | p.Arg196His(p.R196H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504591:140504591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.470T>C |
| AA Mutation | p.Met157Thr(p.M157T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370536 |
| Start | 140503889:140503889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1172G>A |
| AA Mutation | p.Arg391His(p.R391H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504192:140504192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.869C>T |
| AA Mutation | p.Pro290Leu(p.P290L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504378:140504378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.683G>A |
| AA Mutation | p.Gly228Asp(p.G228D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504341:140504341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.720T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504413:140504413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.648G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504473:140504473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.588C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504431:140504431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.630G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370536 |
| Start | 140504663:140504663(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.398delG |
| AA Mutation | p.Gly133ValfsTer7(p.G133Vfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000370536 |
| Start | 140504330:140504350(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs776775669 |
| CDS Mutation | c.711_731delCGCCGCCGCTGCCGCGGCCGC |
| AA Mutation | p.Ala242_Ala248del(p.A242_A248del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |