Primary Site >> Pancreatic Cancer
Gene >> ABCB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265724 |
| Start | 87561356:87561356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.734T>C |
| AA Mutation | p.Leu245Ser(p.L245S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265724 |
| Start | 87544950:87544950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs528939709 |
| CDS Mutation | c.1937G>T |
| AA Mutation | p.Ser646Ile(p.S646I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265724 |
| Start | 87566202:87566202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.570T>G |
| AA Mutation | p.Ile190Met(p.I190M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265724 |
| Start | 87509475:87509475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3289G>T |
| AA Mutation | p.Asp1097Tyr(p.D1097Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000265724 |
| Start | 87509351:87509351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3413G>T |
| AA Mutation | p.Arg1138Leu(p.R1138L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000265724 |
| Start | 87566211:87566211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.561T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |