Primary Site >> Stomach Cancer
Gene >> TUBB6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325852:12325852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751476032 |
| CDS Mutation | c.1063G>A |
| AA Mutation | p.Asp355Asn(p.D355N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325591:12325591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.802C>T |
| AA Mutation | p.Pro268Ser(p.P268S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325460:12325460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.671A>T |
| AA Mutation | p.Asp224Val(p.D224V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325490:12325490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.701G>C |
| AA Mutation | p.Ser234Thr(p.S234T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325151:12325151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368245437 |
| CDS Mutation | c.362G>A |
| AA Mutation | p.Arg121Gln(p.R121Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325750:12325750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.961A>G |
| AA Mutation | p.Met321Val(p.M321V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325561:12325561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.772G>A |
| AA Mutation | p.Val258Met(p.V258M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325878:12325878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1089G>A |
| AA Mutation | p.Met363Ile(p.M363I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12311006:12311006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571214765 |
| CDS Mutation | c.230G>A |
| AA Mutation | p.Arg77Gln(p.R77Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325336:12325336(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.547T>C |
| AA Mutation | p.Tyr183His(p.Y183H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325184:12325184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.395G>A |
| AA Mutation | p.Gly132Asp(p.G132D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325617:12325617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376782121 |
| CDS Mutation | c.828C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317702 |
| Start | 12308307:12308307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.15G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317702 |
| Start | 12325605:12325605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140883153 |
| CDS Mutation | c.816G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |