Primary Site >> Pancreatic Cancer
Gene >> ZNF462
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277225 |
| Start | 106924255:106924255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.343C>T |
| AA Mutation | p.Arg115Cys(p.R115C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277225 |
| Start | 106927115:106927115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764464294 |
| CDS Mutation | c.3203G>A |
| AA Mutation | p.Arg1068Gln(p.R1068Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277225 |
| Start | 106972095:106972095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6518C>A |
| AA Mutation | p.Pro2173His(p.P2173H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277225 |
| Start | 106984191:106984191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6838C>T |
| AA Mutation | p.Arg2280Cys(p.R2280C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000277225 |
| Start | 106929682:106929682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5770C>T |
| AA Mutation | p.Arg1924Cys(p.R1924C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000277225 |
| Start | 106927392:106927392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755889233 |
| CDS Mutation | c.3480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |