Primary Site >> Stomach Cancer
Gene >> RELB
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221452 |
| Start | 45037737:45037737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770578374 |
| CDS Mutation | c.1687C>T |
| AA Mutation | p.Arg563Cys(p.R563C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221452 |
| Start | 45037585:45037585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1535C>G |
| AA Mutation | p.Ala512Gly(p.A512G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221452 |
| Start | 45012190:45012190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.418T>C |
| AA Mutation | p.Phe140Leu(p.F140L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221452 |
| Start | 45032606:45032606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1064G>A |
| AA Mutation | p.Arg355His(p.R355H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221452 |
| Start | 45037456:45037456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1406G>A |
| AA Mutation | p.Gly469Asp(p.G469D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221452 |
| Start | 45022138:45022138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.590G>A |
| AA Mutation | p.Ser197Asn(p.S197N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221452 |
| Start | 45012036:45012036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756636259 |
| CDS Mutation | c.264G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221452 |
| Start | 45012165:45012165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.393G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221452 |
| Start | 45012246:45012246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.474C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221452 |
| Start | 45012198:45012198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770603208 |
| CDS Mutation | c.426C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221452 |
| Start | 45037637:45037637(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770384014 |
| CDS Mutation | c.1587C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |