Primary Site >> Stomach Cancer
Gene >> CASP2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310447 |
| Start | 143294278:143294278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.524A>G |
| AA Mutation | p.Gln175Arg(p.Q175R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000310447 |
| Start | 143294715:143294715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.689T>C |
| AA Mutation | p.Val230Ala(p.V230A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310447 |
| Start | 143304717:143304717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142190608 |
| CDS Mutation | c.1161C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310447 |
| Start | 143292631:143292631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200175061 |
| CDS Mutation | c.408C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310447 |
| Start | 143303845:143303845(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746887367 |
| CDS Mutation | c.1029C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000310447 |
| Start | 143304945:143304945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200701125 |
| CDS Mutation | c.1233C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |