Primary Site >> Stomach Cancer
Gene >> COIL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240316 |
| Start | 56942072:56942072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1610C>T |
| AA Mutation | p.Ala537Val(p.A537V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240316 |
| Start | 56960980:56960980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.40G>T |
| AA Mutation | p.Asp14Tyr(p.D14Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240316 |
| Start | 56939106:56939106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1696T>A |
| AA Mutation | p.Ser566Thr(p.S566T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000240316 |
| Start | 56942063:56942063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1619T>C |
| AA Mutation | p.Val540Ala(p.V540A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000240316 |
| Start | 56950757:56950757(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.485delA |
| AA Mutation | p.Asn162ThrfsTer47(p.N162Tfs*47) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000240316 |
| Start | 56950655:56950655(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs748995811 |
| CDS Mutation | c.587delA |
| AA Mutation | p.Lys196ArgfsTer13(p.K196Rfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000240316 |
| Start | 56950013:56950014(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1228_1229insACACATTCTAA |
| AA Mutation | p.Arg410HisfsTer4(p.R410Hfs*4) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000240316 |
| Start | 56950654:56950655(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.587dupA |
| AA Mutation | p.Ala197GlyfsTer2(p.A197Gfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |