Primary Site >> Pancreatic Cancer
Gene >> TECTA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264037 |
| Start | 121118317:121118317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.802C>T |
| AA Mutation | p.Arg268Trp(p.R268W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264037 |
| Start | 121128120:121128120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776008108 |
| CDS Mutation | c.2143C>T |
| AA Mutation | p.Leu715Phe(p.L715F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264037 |
| Start | 121129641:121129641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2371A>G |
| AA Mutation | p.Asn791Asp(p.N791D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264037 |
| Start | 121157947:121157947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4412C>T |
| AA Mutation | p.Ala1471Val(p.A1471V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264037 |
| Start | 121189873:121189873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6360C>A |
| AA Mutation | p.Ser2120Arg(p.S2120R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264037 |
| Start | 121157965:121157965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527976707 |
| CDS Mutation | c.4430G>A |
| AA Mutation | p.Arg1477His(p.R1477H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264037 |
| Start | 121128176:121128176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs397517145 |
| CDS Mutation | c.2199C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264037 |
| Start | 121152981:121152981(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371771729 |
| CDS Mutation | c.4206C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264037 |
| Start | 121118499:121118499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.984A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264037 |
| Start | 121160302:121160302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764153521 |
| CDS Mutation | c.4857C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264037 |
| Start | 121162303:121162303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762504147 |
| CDS Mutation | c.5205C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |