Primary Site >> Pancreatic Cancer
Gene >> ADAMTS18
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77283961:77283961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3661A>G |
| AA Mutation | p.Ile1221Val(p.I1221V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77319883:77319883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147816593 |
| CDS Mutation | c.2498C>T |
| AA Mutation | p.Ala833Val(p.A833V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000282849 |
| Start | 77356012:77356012(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1388C>T |
| AA Mutation | p.Pro463Leu(p.P463L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000282849 |
| Start | 77367723:77367723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.496T>G |
| AA Mutation | p.Ser166Ala(p.S166A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000282849 |
| Start | 77293148:77293148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3117G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000282849 |
| Start | 77364319:77364319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753594057 |
| CDS Mutation | c.841C>T |
| AA Mutation | p.Arg281Ter(p.R281*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000282849 |
| Start | 77284072:77284072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759235937 |
| CDS Mutation | c.3551-1G>C |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |