Primary Site >> Liver Cancer
Gene >> NID2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216286 |
| Start | 52067912:52067912(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.480G>T |
| AA Mutation | p.Trp160Cys(p.W160C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216286 |
| Start | 52054224:52054224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200644684 |
| CDS Mutation | c.865G>A |
| AA Mutation | p.Ala289Thr(p.A289T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216286 |
| Start | 52015203:52015203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3101C>G |
| AA Mutation | p.Pro1034Arg(p.P1034R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216286 |
| Start | 52020131:52020131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2722T>A |
| AA Mutation | p.Tyr908Asn(p.Y908N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216286 |
| Start | 52068913:52068913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.82G>C |
| AA Mutation | p.Ala28Pro(p.A28P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216286 |
| Start | 52015201:52015201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780404034 |
| CDS Mutation | c.3103C>T |
| AA Mutation | p.Arg1035Trp(p.R1035W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216286 |
| Start | 52019210:52019210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2879T>A |
| AA Mutation | p.Ile960Asn(p.I960N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216286 |
| Start | 52042342:52042342(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1588C>A |
| AA Mutation | p.His530Asn(p.H530N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216286 |
| Start | 52053775:52053775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1233A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216286 |
| Start | 52019197:52019197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142814187 |
| CDS Mutation | c.2892C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |