Primary Site >> Stomach Cancer
Gene >> CEACAM1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000161559 |
| Start | 42521953:42521953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.674G>T |
| AA Mutation | p.Arg225Leu(p.R225L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000161559 |
| Start | 42511611:42511611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1394A>G |
| AA Mutation | p.Asp465Gly(p.D465G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000161559 |
| Start | 42519016:42519016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138618516 |
| CDS Mutation | c.1178C>T |
| AA Mutation | p.Thr393Met(p.T393M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000161559 |
| Start | 42521477:42521477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775600985 |
| CDS Mutation | c.748C>T |
| AA Mutation | p.Arg250Cys(p.R250C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000161559 |
| Start | 42519145:42519145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1049C>T |
| AA Mutation | p.Thr350Ile(p.T350I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000161559 |
| Start | 42528364:42528364(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.11T>G |
| AA Mutation | p.Leu4Arg(p.L4R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000161559 |
| Start | 42519125:42519125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1069A>C |
| AA Mutation | p.Ile357Leu(p.I357L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000161559 |
| Start | 42522136:42522136(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768241278 |
| CDS Mutation | c.491C>T |
| AA Mutation | p.Ala164Val(p.A164V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000161559 |
| Start | 42511622:42511622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767345563 |
| CDS Mutation | c.1383C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000161559 |
| Start | 42527132:42527132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760963879 |
| CDS Mutation | c.333C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |