Primary Site >> Liver Cancer
Gene >> HSPG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21836874:21836874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10283G>A |
| AA Mutation | p.Gly3428Asp(p.G3428D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21874910:21874910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3395A>T |
| AA Mutation | p.Tyr1132Phe(p.Y1132F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21831756:21831756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.11248A>G |
| AA Mutation | p.Thr3750Ala(p.T3750A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21890090:21890090(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.465T>A |
| AA Mutation | p.Asn155Lys(p.N155K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000374695 |
| Start | 21895923:21895923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.243G>A |
| AA Mutation | p.Met81Ile(p.M81I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21846546:21846546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545072429 |
| CDS Mutation | c.8218G>A |
| AA Mutation | p.Glu2740Lys(p.E2740K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374695 |
| Start | 21854330:21854330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369444110 |
| CDS Mutation | c.6302G>A |
| AA Mutation | p.Arg2101His(p.R2101H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000374695 |
| Start | 21833366:21833379(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.10984_10997delGTGGTGCCCTACTT |
| AA Mutation | p.Val3662HisfsTer109(p.V3662Hfs*109) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |