Primary Site >> Pancreatic Cancer
Gene >> TEP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20373526:20373526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146330073 |
| CDS Mutation | c.6662G>A |
| AA Mutation | p.Arg2221Gln(p.R2221Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20375766:20375766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6352G>A |
| AA Mutation | p.Asp2118Asn(p.D2118N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20382021:20382021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754265798 |
| CDS Mutation | c.4316G>A |
| AA Mutation | p.Arg1439Gln(p.R1439Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000262715 |
| Start | 20404742:20404742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144854568 |
| CDS Mutation | c.901G>A |
| AA Mutation | p.Val301Ile(p.V301I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20383249:20383249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3972T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20373062:20373062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776756458 |
| CDS Mutation | c.6900A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000262715 |
| Start | 20373065:20373065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6897T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |