Primary Site >> Liver Cancer
Gene >> SLIT3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 169300669:169300669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.41C>G |
| AA Mutation | p.Ala14Gly(p.A14G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168817428:168817428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.665A>T |
| AA Mutation | p.His222Leu(p.H222L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 169300517:169300517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.193C>A |
| AA Mutation | p.Arg65Ser(p.R65S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168749478:168749478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2131T>A |
| AA Mutation | p.Cys711Ser(p.C711S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000519560 |
| Start | 168753043:168753043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1885A>T |
| AA Mutation | p.Ser629Cys(p.S629C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168692624:168692624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3159C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168696353:168696353(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3021C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168762631:168762631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776500729 |
| CDS Mutation | c.1518C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168708066:168708066(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2754T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168687038:168687038(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143708971 |
| CDS Mutation | c.3255C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000519560 |
| Start | 168762658:168762658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187066924 |
| CDS Mutation | c.1491C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |