Primary Site >> Stomach Cancer
Gene >> SCGN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377961 |
| Start | 25670036:25670036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.431C>T |
| AA Mutation | p.Ala144Val(p.A144V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377961 |
| Start | 25664985:25664985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.289C>A |
| AA Mutation | p.Leu97Ile(p.L97I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377961 |
| Start | 25681981:25681981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148850055 |
| CDS Mutation | c.502C>T |
| AA Mutation | p.Arg168Trp(p.R168W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377961 |
| Start | 25670005:25670005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.400C>A |
| AA Mutation | p.Leu134Ile(p.L134I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377961 |
| Start | 25689478:25689478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.579T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377961 |
| Start | 25665017:25665017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140955997 |
| CDS Mutation | c.321C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |