Primary Site >> Stomach Cancer
Gene >> SEMA4B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411539 |
| Start | 90227588:90227588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201809168 |
| CDS Mutation | c.1720G>A |
| AA Mutation | p.Ala574Thr(p.A574T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411539 |
| Start | 90227606:90227606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779317447 |
| CDS Mutation | c.1738G>A |
| AA Mutation | p.Ala580Thr(p.A580T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411539 |
| Start | 90228411:90228411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2282G>A |
| AA Mutation | p.Cys761Tyr(p.C761Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411539 |
| Start | 90227613:90227613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200793183 |
| CDS Mutation | c.1745C>T |
| AA Mutation | p.Ser582Leu(p.S582L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411539 |
| Start | 90223584:90223584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.887T>C |
| AA Mutation | p.Leu296Pro(p.L296P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000411539 |
| Start | 90228344:90228344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201550724 |
| CDS Mutation | c.2215C>T |
| AA Mutation | p.Arg739Trp(p.R739W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000411539 |
| Start | 90223619:90223619(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.922C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000411539 |
| Start | 90225051:90225051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1278C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000411539 |
| Start | 90221756:90221756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370338036 |
| CDS Mutation | c.852C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |