Primary Site >> Pancreatic Cancer
Gene >> MUC17
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101040670:101040670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769024651 |
| CDS Mutation | c.9254C>T |
| AA Mutation | p.Ser3085Leu(p.S3085L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101035939:101035939(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374713003 |
| CDS Mutation | c.4523C>T |
| AA Mutation | p.Thr1508Met(p.T1508M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101034256:101034256(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2840C>G |
| AA Mutation | p.Thr947Ser(p.T947S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101020187:101020187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.52C>A |
| AA Mutation | p.Leu18Ile(p.L18I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101032966:101032966(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1550C>T |
| AA Mutation | p.Ser517Phe(p.S517F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101036559:101036559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149023842 |
| CDS Mutation | c.5143G>A |
| AA Mutation | p.Val1715Ile(p.V1715I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306151 |
| Start | 101043760:101043760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756321309 |
| CDS Mutation | c.12344C>T |
| AA Mutation | p.Thr4115Met(p.T4115M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101048855:101048855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753376856 |
| CDS Mutation | c.12546G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306151 |
| Start | 101037725:101037725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6309A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000306151 |
| Start | 101036486:101036486(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.5070delT |
| AA Mutation | p.Pro1691LeufsTer2(p.P1691Lfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |