Primary Site >> Pancreatic Cancer
Gene >> ITIH5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576707:7576707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761012253 |
| CDS Mutation | c.1724G>A |
| AA Mutation | p.Arg575His(p.R575H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7563150:7563150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2762A>C |
| AA Mutation | p.Asp921Ala(p.D921A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7576971:7576971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112992012 |
| CDS Mutation | c.1460G>A |
| AA Mutation | p.Arg487His(p.R487H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7640807:7640807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.348G>T |
| AA Mutation | p.Lys116Asn(p.K116N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000397146 |
| Start | 7641997:7641997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.229G>A |
| AA Mutation | p.Ala77Thr(p.A77T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000397146 |
| Start | 7637268:7637268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.612G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |