Primary Site >> Stomach Cancer
Gene >> CD276
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318443 |
| Start | 73704224:73704224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778780413 |
| CDS Mutation | c.1121G>A |
| AA Mutation | p.Arg374Gln(p.R374Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318443 |
| Start | 73702317:73702317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.142C>A |
| AA Mutation | p.Leu48Met(p.L48M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318443 |
| Start | 73702483:73702483(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.308G>A |
| AA Mutation | p.Gly103Asp(p.G103D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318443 |
| Start | 73703973:73703973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780867163 |
| CDS Mutation | c.1048G>A |
| AA Mutation | p.Ala350Thr(p.A350T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318443 |
| Start | 73702949:73702949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.596A>G |
| AA Mutation | p.Gln199Arg(p.Q199R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318443 |
| Start | 73699646:73699646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770116040 |
| CDS Mutation | c.7C>T |
| AA Mutation | p.Arg3Cys(p.R3C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318443 |
| Start | 73704336:73704336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776236542 |
| CDS Mutation | c.1233G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318443 |
| Start | 73702929:73702929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775878704 |
| CDS Mutation | c.576G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318443 |
| Start | 73703948:73703948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766977760 |
| CDS Mutation | c.1023C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318443 |
| Start | 73703978:73703978(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745660933 |
| CDS Mutation | c.1053C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |