Primary Site >> Stomach Cancer
Gene >> CD320
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301458 |
| Start | 8302534:8302534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372399234 |
| CDS Mutation | c.778C>T |
| AA Mutation | p.Arg260Cys(p.R260C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301458 |
| Start | 8305076:8305076(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.223G>C |
| AA Mutation | p.Asp75His(p.D75H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301458 |
| Start | 8302533:8302533(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370038440 |
| CDS Mutation | c.779G>A |
| AA Mutation | p.Arg260His(p.R260H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301458 |
| Start | 8302599:8302599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.713T>C |
| AA Mutation | p.Leu238Pro(p.L238P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301458 |
| Start | 8305099:8305099(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.200G>A |
| AA Mutation | p.Cys67Tyr(p.C67Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301458 |
| Start | 8303906:8303906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769150463 |
| CDS Mutation | c.451C>T |
| AA Mutation | p.Arg151Cys(p.R151C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |