Primary Site >> Stomach Cancer
Gene >> CACUL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369151 |
| Start | 118707559:118707559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.626G>T |
| AA Mutation | p.Arg209Ile(p.R209I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369151 |
| Start | 118701344:118701344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.758C>T |
| AA Mutation | p.Thr253Met(p.T253M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369151 |
| Start | 118701402:118701402(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.700T>C |
| AA Mutation | p.Phe234Leu(p.F234L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369151 |
| Start | 118754598:118754598(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.165delG |
| AA Mutation | p.Gln56SerfsTer32(p.Q56Sfs*32) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369151 |
| Start | 118754442:118754442(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.321delC |
| AA Mutation | p.Thr108ProfsTer16(p.T108Pfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000369151 |
| Start | 118730367:118730367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.411G>A |
| AA Mutation | p.Trp137Ter(p.W137*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369151 |
| Start | 118754597:118754598(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs747095390 |
| CDS Mutation | c.165dupG |
| AA Mutation | p.Gln56AlafsTer30(p.Q56Afs*30) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |