Primary Site >> Stomach Cancer
Gene >> CEACAM7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006724 |
| Start | 41683817:41683817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.674G>C |
| AA Mutation | p.Ser225Thr(p.S225T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006724 |
| Start | 41687024:41687024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.262C>A |
| AA Mutation | p.Gln88Lys(p.Q88K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006724 |
| Start | 41687191:41687191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.95A>G |
| AA Mutation | p.Asn32Ser(p.N32S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000006724 |
| Start | 41677472:41677472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782548650 |
| CDS Mutation | c.738C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000006724 |
| Start | 41683876:41683876(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200263190 |
| CDS Mutation | c.615C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000006724 |
| Start | 41687054:41687054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782719770 |
| CDS Mutation | c.232C>T |
| AA Mutation | p.Arg78Ter(p.R78*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |