Primary Site >> Liver Cancer
Gene >> ACAN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439576 |
| Start | 88854892:88854892(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2307G>C |
| AA Mutation | p.Glu769Asp(p.E769D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439576 |
| Start | 88845573:88845573(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1120A>G |
| AA Mutation | p.Thr374Ala(p.T374A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439576 |
| Start | 88841784:88841784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.674A>G |
| AA Mutation | p.Asp225Gly(p.D225G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439576 |
| Start | 88858251:88858251(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5666C>T |
| AA Mutation | p.Ser1889Phe(p.S1889F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439576 |
| Start | 88859216:88859216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs533925391 |
| CDS Mutation | c.6631G>A |
| AA Mutation | p.Val2211Ile(p.V2211I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000439576 |
| Start | 88859279:88859279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6694A>G |
| AA Mutation | p.Thr2232Ala(p.T2232A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000439576 |
| Start | 88873951:88873951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7443C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000439576 |
| Start | 88858342:88858342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778250246 |
| CDS Mutation | c.5757G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |