Primary Site >> Stomach Cancer
Gene >> BCL6B
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293805 |
| Start | 7026993:7026993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1229A>C |
| AA Mutation | p.Lys410Thr(p.K410T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293805 |
| Start | 7026750:7026750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1100G>A |
| AA Mutation | p.Arg367Gln(p.R367Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293805 |
| Start | 7024171:7024171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.268G>A |
| AA Mutation | p.Ala90Thr(p.A90T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293805 |
| Start | 7024492:7024492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765843482 |
| CDS Mutation | c.493G>A |
| AA Mutation | p.Glu165Lys(p.E165K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293805 |
| Start | 7024160:7024160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546801346 |
| CDS Mutation | c.257C>T |
| AA Mutation | p.Ala86Val(p.A86V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000293805 |
| Start | 7027546:7027546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769964987 |
| CDS Mutation | c.1367G>A |
| AA Mutation | p.Arg456Gln(p.R456Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000293805 |
| Start | 7024269:7024269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.366C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000293805 |
| Start | 7023806:7023806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs556103118 |
| CDS Mutation | c.135C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000293805 |
| Start | 7024155:7024155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.252C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000293805 |
| Start | 7024131:7024131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.228C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000293805 |
| Start | 7023749:7023749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770426680 |
| CDS Mutation | c.78C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000293805 |
| Start | 7026527:7026527(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.960T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000293805 |
| Start | 7024524:7024524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.525A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000293805 |
| Start | 7027608:7027608(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1434delG |
| AA Mutation | p.Ter480SerfsTer2(p.*480Sfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000293805 |
| Start | 7024539:7024539(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.546delC |
| AA Mutation | p.Ser183ValfsTer20(p.S183Vfs*20) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000293805 |
| Start | 7024581:7024581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.582G>A |
| AA Mutation | p.Trp194Ter(p.W194*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000293805 |
| Start | 7024538:7024539(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs780109291 |
| CDS Mutation | c.546dupC |
| AA Mutation | p.Ser183GlnfsTer6(p.S183Qfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |