Primary Site >> Stomach Cancer
Gene >> TACC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317827 |
| Start | 38819660:38819660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.416C>A |
| AA Mutation | p.Pro139His(p.P139H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317827 |
| Start | 38836264:38836264(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775926435 |
| CDS Mutation | c.1816G>A |
| AA Mutation | p.Val606Met(p.V606M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317827 |
| Start | 38847993:38847993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2388G>T |
| AA Mutation | p.Glu796Asp(p.E796D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317827 |
| Start | 38842361:38842361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2035G>A |
| AA Mutation | p.Ala679Thr(p.A679T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317827 |
| Start | 38846769:38846769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149836912 |
| CDS Mutation | c.2299C>T |
| AA Mutation | p.Arg767Cys(p.R767C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000317827 |
| Start | 38819812:38819812(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760101311 |
| CDS Mutation | c.568G>A |
| AA Mutation | p.Ala190Thr(p.A190T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317827 |
| Start | 38827278:38827278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1563C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317827 |
| Start | 38836200:38836200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754110202 |
| CDS Mutation | c.1752G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000317827 |
| Start | 38831141:38831141(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760358625 |
| CDS Mutation | c.1677G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000317827 |
| Start | 38819800:38819801(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.561_571dupGCCAGACGCCC |
| AA Mutation | p.Leu191ArgfsTer10(p.L191Rfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |