Primary Site >> Stomach Cancer
Gene >> CIR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342016 |
| Start | 174378943:174378943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768225837 |
| CDS Mutation | c.464C>T |
| AA Mutation | p.Ser155Leu(p.S155L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000342016 |
| Start | 174387751:174387751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.101A>G |
| AA Mutation | p.Tyr34Cys(p.Y34C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342016 |
| Start | 174348857:174348857(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.993A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342016 |
| Start | 174348680:174348680(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000342016 |
| Start | 174351718:174351718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763864312 |
| CDS Mutation | c.492G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000342016 |
| Start | 174348985:174348985(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs752412345 |
| CDS Mutation | c.865delA |
| AA Mutation | p.Ile289TyrfsTer51(p.I289Yfs*51) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000342016 |
| Start | 174351663:174351663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753602814 |
| CDS Mutation | c.547C>T |
| AA Mutation | p.Arg183Ter(p.R183*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |