Primary Site >> Liver Cancer
Gene >> IGF1R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98891596:98891596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.912G>A |
| AA Mutation | p.Met304Ile(p.M304I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98922272:98922272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2326C>A |
| AA Mutation | p.Pro776Thr(p.P776T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98923967:98923967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2577T>A |
| AA Mutation | p.Asn859Lys(p.N859K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98935326:98935326(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3197T>A |
| AA Mutation | p.Leu1066Gln(p.L1066Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98916098:98916098(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143193096 |
| CDS Mutation | c.1963G>A |
| AA Mutation | p.Gly655Ser(p.G655S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98948640:98948640(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3654C>G |
| AA Mutation | p.Asn1218Lys(p.N1218K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98916855:98916855(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2180A>G |
| AA Mutation | p.His727Arg(p.H727R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98911425:98911425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201778894 |
| CDS Mutation | c.1573G>A |
| AA Mutation | p.Val525Ile(p.V525I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98707934:98707934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.467A>T |
| AA Mutation | p.Asp156Val(p.D156V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98939284:98939284(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3381C>A |
| AA Mutation | p.Asn1127Lys(p.N1127K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98707804:98707804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.337T>C |
| AA Mutation | p.Tyr113His(p.Y113H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268035 |
| Start | 98916048:98916048(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144533252 |
| CDS Mutation | c.1913A>G |
| AA Mutation | p.Asn638Ser(p.N638S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268035 |
| Start | 98908700:98908700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542546475 |
| CDS Mutation | c.1263C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |