Primary Site >> Liver Cancer
Gene >> TLL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000061240 |
| Start | 166065858:166065858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2183T>C |
| AA Mutation | p.Phe728Ser(p.F728S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000061240 |
| Start | 166057229:166057229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750536542 |
| CDS Mutation | c.1766G>A |
| AA Mutation | p.Arg589Gln(p.R589Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000061240 |
| Start | 166078028:166078028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2440T>A |
| AA Mutation | p.Leu814Ile(p.L814I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000061240 |
| Start | 166099355:166099355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2735C>A |
| AA Mutation | p.Pro912Gln(p.P912Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000061240 |
| Start | 166074984:166074984(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2295T>A |
| AA Mutation | p.Asn765Lys(p.N765K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000061240 |
| Start | 166099410:166099410(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2790A>T |
| AA Mutation | p.Glu930Asp(p.E930D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000061240 |
| Start | 166065782:166065782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2107T>C |
| AA Mutation | p.Ser703Pro(p.S703P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000061240 |
| Start | 166060155:166060155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1974G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000061240 |
| Start | 166055246:166055246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758162833 |
| CDS Mutation | c.1695A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000061240 |
| Start | 166055201:166055201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766550068 |
| CDS Mutation | c.1650T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000061240 |
| Start | 166065744:166065748(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2069_2073delGCAAA |
| AA Mutation | p.Gly690ValfsTer5(p.G690Vfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |