Primary Site >> Stomach Cancer
Gene >> CD22
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000085219 |
| Start | 35332630:35332630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756111081 |
| CDS Mutation | c.118G>A |
| AA Mutation | p.Val40Ile(p.V40I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000085219 |
| Start | 35341519:35341519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1684T>A |
| AA Mutation | p.Ser562Thr(p.S562T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000085219 |
| Start | 35337860:35337860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.824C>T |
| AA Mutation | p.Thr275Met(p.T275M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000085219 |
| Start | 35345613:35345613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2220C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000085219 |
| Start | 35341077:35341077(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775643440 |
| CDS Mutation | c.1446C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000085219 |
| Start | 35337888:35337888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.852C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000085219 |
| Start | 35332764:35332764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.252G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000085219 |
| Start | 35341011:35341011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752070697 |
| CDS Mutation | c.1380C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000085219 |
| Start | 35341447:35341447(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1612G>T |
| AA Mutation | p.Glu538Ter(p.E538*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000085219 |
| Start | 35341345:35341346(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs775671966 |
| CDS Mutation | c.1516dupC |
| AA Mutation | p.Arg506ProfsTer25(p.R506Pfs*25) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |