Primary Site >> Stomach Cancer
Gene >> SPON2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290902 |
| Start | 1172052:1172052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.20C>T |
| AA Mutation | p.Ala7Val(p.A7V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290902 |
| Start | 1170477:1170477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.736C>G |
| AA Mutation | p.Gln246Glu(p.Q246E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290902 |
| Start | 1170486:1170486(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776991535 |
| CDS Mutation | c.727C>T |
| AA Mutation | p.Arg243Trp(p.R243W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000290902 |
| Start | 1170408:1170408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746452833 |
| CDS Mutation | c.805G>A |
| AA Mutation | p.Ala269Thr(p.A269T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290902 |
| Start | 1171482:1171482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141880428 |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290902 |
| Start | 1171871:1171871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.201G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000290902 |
| Start | 1171371:1171371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745460257 |
| CDS Mutation | c.336G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000290902 |
| Start | 1171874:1171875(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs775922429 |
| CDS Mutation | c.197dupC |
| AA Mutation | p.Ala67CysfsTer12(p.A67Cfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |