Primary Site >> Pancreatic Cancer
Gene >> TSC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219476 |
| Start | 2086296:2086296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373635516 |
| CDS Mutation | c.4766C>T |
| AA Mutation | p.Pro1589Leu(p.P1589L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219476 |
| Start | 2070559:2070559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397515296 |
| CDS Mutation | c.1820C>T |
| AA Mutation | p.Ala607Val(p.A607V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000219476 |
| Start | 2079278:2079278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3134C>T |
| AA Mutation | p.Ser1045Phe(p.S1045F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219476 |
| Start | 2084251:2084251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4029G>T |
| AA Mutation | p.Glu1343Asp(p.E1343D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219476 |
| Start | 2086298:2086298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4768G>A |
| AA Mutation | p.Asp1590Asn(p.D1590N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000219476 |
| Start | 2057129:2057129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.799C>A |
| AA Mutation | p.His267Asn(p.H267N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219476 |
| Start | 2062581:2062581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1342C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219476 |
| Start | 2074211:2074211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2367C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000219476 |
| Start | 2080328:2080328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3561G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |