Primary Site >> Pancreatic Cancer
Gene >> SPEN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375759 |
| Start | 15937824:15937824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10522G>A |
| AA Mutation | p.Val3508Met(p.V3508M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375759 |
| Start | 15928128:15928128(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749814808 |
| CDS Mutation | c.1888C>T |
| AA Mutation | p.Arg630Cys(p.R630C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375759 |
| Start | 15928668:15928668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2428C>T |
| AA Mutation | p.Arg810Trp(p.R810W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375759 |
| Start | 15937909:15937909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762946669 |
| CDS Mutation | c.10607G>A |
| AA Mutation | p.Arg3536Gln(p.R3536Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375759 |
| Start | 15931961:15931961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5721C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375759 |
| Start | 15931436:15931442(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5196_5202delTGCCAAG |
| AA Mutation | p.Ala1733LeufsTer15(p.A1733Lfs*15) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000375759 |
| Start | 15935523:15935523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9283C>T |
| AA Mutation | p.Gln3095Ter(p.Q3095*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |