Primary Site >> Pancreatic Cancer
Gene >> PTPRH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376350 |
| Start | 55198754:55198754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1579G>T |
| AA Mutation | p.Gly527Cys(p.G527C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376350 |
| Start | 55185553:55185553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367681827 |
| CDS Mutation | c.3011G>A |
| AA Mutation | p.Arg1004Gln(p.R1004Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376350 |
| Start | 55197399:55197399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1708G>A |
| AA Mutation | p.Asp570Asn(p.D570N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000376350 |
| Start | 55202269:55202269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754481794 |
| CDS Mutation | c.940G>A |
| AA Mutation | p.Ala314Thr(p.A314T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376350 |
| Start | 55200246:55200246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1410C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000376350 |
| Start | 55197139:55197139(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775338442 |
| CDS Mutation | c.1968G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |