Primary Site >> Stomach Cancer
Gene >> MAGEB6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194411:26194411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142927857 |
| CDS Mutation | c.565C>T |
| AA Mutation | p.Arg189Cys(p.R189C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194522:26194522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200923993 |
| CDS Mutation | c.676C>T |
| AA Mutation | p.Arg226Cys(p.R226C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379034 |
| Start | 26193982:26193982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775309752 |
| CDS Mutation | c.136C>T |
| AA Mutation | p.Arg46Cys(p.R46C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194748:26194748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781192763 |
| CDS Mutation | c.902G>A |
| AA Mutation | p.Cys301Tyr(p.C301Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194400:26194400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.554T>C |
| AA Mutation | p.Ile185Thr(p.I185T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194780:26194780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.934G>A |
| AA Mutation | p.Gly312Ser(p.G312S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194879:26194879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1033C>T |
| AA Mutation | p.Arg345Trp(p.R345W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194264:26194264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.418C>A |
| AA Mutation | p.His140Asn(p.H140N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194412:26194412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749932015 |
| CDS Mutation | c.566G>A |
| AA Mutation | p.Arg189His(p.R189H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194356:26194356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746794376 |
| CDS Mutation | c.510C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379034 |
| Start | 26193972:26193972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.126A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379034 |
| Start | 26193996:26193996(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.150T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194344:26194344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.498T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379034 |
| Start | 26193921:26193921(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.75C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379034 |
| Start | 26193861:26193861(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379034 |
| Start | 26194383:26194383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148547775 |
| CDS Mutation | c.537C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |