Primary Site >> Pancreatic Cancer
Gene >> MUC6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421673 |
| Start | 1025023:1025023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771070829 |
| CDS Mutation | c.3046C>T |
| AA Mutation | p.Arg1016Cys(p.R1016C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421673 |
| Start | 1028027:1028027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1786C>A |
| AA Mutation | p.Leu596Met(p.L596M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421673 |
| Start | 1028689:1028689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1548G>T |
| AA Mutation | p.Gln516His(p.Q516H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421673 |
| Start | 1029525:1029525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1106G>T |
| AA Mutation | p.Gly369Val(p.G369V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000421673 |
| Start | 1031906:1031906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547156930 |
| CDS Mutation | c.263G>A |
| AA Mutation | p.Arg88Gln(p.R88Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000421673 |
| Start | 1025891:1025892(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.2712dupA |
| AA Mutation | p.Gln905ThrfsTer189(p.Q905Tfs*189) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000421673 |
| Start | 1016412:1016414(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs765184193 |
| CDS Mutation | c.6387_6389delCTC |
| AA Mutation | p.Ser2130del(p.S2130del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |