Primary Site >> Stomach Cancer
Gene >> TUBB3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315491 |
| Start | 89934897:89934897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.446C>T |
| AA Mutation | p.Thr149Met(p.T149M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935620:89935620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1169G>A |
| AA Mutation | p.Arg390Gln(p.R390Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315491 |
| Start | 89934918:89934918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.467G>A |
| AA Mutation | p.Arg156His(p.R156H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935238:89935238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.787C>G |
| AA Mutation | p.Leu263Val(p.L263V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315491 |
| Start | 89934935:89934935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.484C>T |
| AA Mutation | p.Arg162Cys(p.R162C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935409:89935409(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.958C>T |
| AA Mutation | p.Arg320Cys(p.R320C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935679:89935679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs267607165 |
| CDS Mutation | c.1228G>A |
| AA Mutation | p.Glu410Lys(p.E410K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935505:89935505(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1054G>A |
| AA Mutation | p.Ala352Thr(p.A352T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935507:89935507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201308325 |
| CDS Mutation | c.1056C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935567:89935567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566062002 |
| CDS Mutation | c.1116G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315491 |
| Start | 89932603:89932603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369355135 |
| CDS Mutation | c.90C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935735:89935735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935108:89935108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778395569 |
| CDS Mutation | c.657G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000315491 |
| Start | 89935263:89935263(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.817delC |
| AA Mutation | p.Leu273SerfsTer12(p.L273Sfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |