Primary Site >> Stomach Cancer
Gene >> TSKU
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333090 |
| Start | 76796392:76796392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.776T>A |
| AA Mutation | p.Leu259Gln(p.L259Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333090 |
| Start | 76795917:76795917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.301C>G |
| AA Mutation | p.Pro101Ala(p.P101A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333090 |
| Start | 76796211:76796211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.595G>T |
| AA Mutation | p.Val199Leu(p.V199L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333090 |
| Start | 76796208:76796208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.592G>A |
| AA Mutation | p.Ala198Thr(p.A198T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333090 |
| Start | 76796482:76796482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758698062 |
| CDS Mutation | c.866C>T |
| AA Mutation | p.Thr289Ile(p.T289I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000333090 |
| Start | 76796591:76796591(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.979delC |
| AA Mutation | p.Arg327GlyfsTer14(p.R327Gfs*14) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |