Primary Site >> Liver Cancer
Gene >> NOTCH2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119925425:119925425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4391C>T |
| AA Mutation | p.Ala1464Val(p.A1464V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119920348:119920348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5360G>A |
| AA Mutation | p.Arg1787Gln(p.R1787Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119941736:119941736(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2771G>T |
| AA Mutation | p.Gly924Val(p.G924V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119937380:119937380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3424A>G |
| AA Mutation | p.Thr1142Ala(p.T1142A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119987074:119987074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.760G>A |
| AA Mutation | p.Gly254Arg(p.G254R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119919560:119919560(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5533A>C |
| AA Mutation | p.Ser1845Arg(p.S1845R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256646 |
| Start | 119997304:119997304(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587603360 |
| CDS Mutation | c.444C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256646 |
| Start | 119916295:119916296(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.6426_6427insTT |
| AA Mutation | p.Glu2143LeufsTer5(p.E2143Lfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |