Primary Site >> Liver Cancer
Gene >> SIGLEC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3694304:3694304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3173T>A |
| AA Mutation | p.Met1058Lys(p.M1058K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3694442:3694442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766676495 |
| CDS Mutation | c.3035C>T |
| AA Mutation | p.Pro1012Leu(p.P1012L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3694287:3694287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3190G>A |
| AA Mutation | p.Val1064Ile(p.V1064I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3699298:3699298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756452334 |
| CDS Mutation | c.1690G>T |
| AA Mutation | p.Ala564Ser(p.A564S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3688567:3688567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5123T>A |
| AA Mutation | p.Leu1708Gln(p.L1708Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344754 |
| Start | 3692665:3692665(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760676443 |
| CDS Mutation | c.3886C>T |
| AA Mutation | p.His1296Tyr(p.H1296Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3693613:3693613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3342G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3703910:3703910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.888C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000344754 |
| Start | 3693085:3693085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144602570 |
| CDS Mutation | c.3555C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |