Primary Site >> Stomach Cancer
Gene >> CD33
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262262 |
| Start | 51225546:51225546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.366A>C |
| AA Mutation | p.Arg122Ser(p.R122S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262262 |
| Start | 51225252:51225252(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.72A>T |
| AA Mutation | p.Gln24His(p.Q24H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262262 |
| Start | 51225364:51225364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138300409 |
| CDS Mutation | c.184C>T |
| AA Mutation | p.Arg62Trp(p.R62W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262262 |
| Start | 51235198:51235198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.787G>A |
| AA Mutation | p.Gly263Arg(p.G263R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262262 |
| Start | 51226344:51226344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.733G>A |
| AA Mutation | p.Gly245Arg(p.G245R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262262 |
| Start | 51225436:51225436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.256A>G |
| AA Mutation | p.Thr86Ala(p.T86A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262262 |
| Start | 51225839:51225839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376172530 |
| CDS Mutation | c.455C>T |
| AA Mutation | p.Thr152Ile(p.T152I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262262 |
| Start | 51239661:51239661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61736476 |
| CDS Mutation | c.1068C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |