Primary Site >> Pancreatic Cancer
Gene >> ITGB4
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000200181 |
| Start | 75727855:75727855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.469G>A |
| AA Mutation | p.Ala157Thr(p.A157T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75730464:75730464(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.962C>A |
| AA Mutation | p.Pro321His(p.P321H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75730955:75730955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1083G>T |
| AA Mutation | p.Glu361Asp(p.E361D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75749011:75749011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3282G>T |
| AA Mutation | p.Gln1094His(p.Q1094H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75756504:75756504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4784C>A |
| AA Mutation | p.Ser1595Tyr(p.S1595Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75752513:75752513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4044G>A |
| AA Mutation | p.Met1348Ile(p.M1348I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000200181 |
| Start | 75732185:75732185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1400G>T |
| AA Mutation | p.Arg467Leu(p.R467L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |