Primary Site >> Pancreatic Cancer
Gene >> LTBP4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308370 |
| Start | 40617218:40617218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3264C>G |
| AA Mutation | p.His1088Gln(p.H1088Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308370 |
| Start | 40613952:40613952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2795G>A |
| AA Mutation | p.Ser932Asn(p.S932N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308370 |
| Start | 40623015:40623015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs34051360 |
| CDS Mutation | c.3751C>T |
| AA Mutation | p.Arg1251Trp(p.R1251W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308370 |
| Start | 40629476:40629476(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4801C>T |
| AA Mutation | p.Arg1601Cys(p.R1601C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308370 |
| Start | 40611387:40611387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2247C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308370 |
| Start | 40619420:40619420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3345C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |