Primary Site >> Stomach Cancer
Gene >> CEACAM8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244336 |
| Start | 42593579:42593579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386T>A |
| AA Mutation | p.Leu129His(p.L129H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244336 |
| Start | 42588999:42588999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.743A>T |
| AA Mutation | p.Tyr248Phe(p.Y248F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244336 |
| Start | 42583316:42583316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.980C>A |
| AA Mutation | p.Ser327Tyr(p.S327Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244336 |
| Start | 42593894:42593894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.71T>G |
| AA Mutation | p.Leu24Arg(p.L24R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000244336 |
| Start | 42593876:42593876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.89C>T |
| AA Mutation | p.Pro30Leu(p.P30L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000244336 |
| Start | 42588989:42588989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.753A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000244336 |
| Start | 42589541:42589541(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765754935 |
| CDS Mutation | c.619A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |