Primary Site >> Stomach Cancer
Gene >> BCL11B
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000357195 |
| Start | 99257471:99257471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.427G>T |
| AA Mutation | p.Gly143Trp(p.G143W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357195 |
| Start | 99174945:99174945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1891G>A |
| AA Mutation | p.Gly631Arg(p.G631R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357195 |
| Start | 99231471:99231471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557598154 |
| CDS Mutation | c.514C>T |
| AA Mutation | p.Arg172Cys(p.R172C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357195 |
| Start | 99175101:99175101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1735G>A |
| AA Mutation | p.Ala579Thr(p.A579T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357195 |
| Start | 99231470:99231470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770333002 |
| CDS Mutation | c.515G>A |
| AA Mutation | p.Arg172His(p.R172H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357195 |
| Start | 99175145:99175145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1691G>A |
| AA Mutation | p.Arg564His(p.R564H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357195 |
| Start | 99175911:99175911(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.925C>T |
| AA Mutation | p.Arg309Cys(p.R309C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357195 |
| Start | 99175365:99175365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1471G>A |
| AA Mutation | p.Gly491Arg(p.G491R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357195 |
| Start | 99257585:99257585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.313G>A |
| AA Mutation | p.Glu105Lys(p.E105K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357195 |
| Start | 99174737:99174737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115625258 |
| CDS Mutation | c.2099C>T |
| AA Mutation | p.Ala700Val(p.A700V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357195 |
| Start | 99176065:99176065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.771C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357195 |
| Start | 99175576:99175576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1260G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357195 |
| Start | 99175093:99175093(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1743C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357195 |
| Start | 99176119:99176119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775384332 |
| CDS Mutation | c.717C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357195 |
| Start | 99231373:99231373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.612T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357195 |
| Start | 99174817:99174817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777226398 |
| CDS Mutation | c.2019C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357195 |
| Start | 99174991:99174991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369506800 |
| CDS Mutation | c.1845C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |