Primary Site >> Liver Cancer
Gene >> ATAD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287394 |
| Start | 123328425:123328425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3633T>A |
| AA Mutation | p.Asp1211Glu(p.D1211E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287394 |
| Start | 123371292:123371292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.583C>T |
| AA Mutation | p.Arg195Cys(p.R195C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287394 |
| Start | 123357683:123357683(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1436C>T |
| AA Mutation | p.Ala479Val(p.A479V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287394 |
| Start | 123328208:123328208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3850G>A |
| AA Mutation | p.Asp1284Asn(p.D1284N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287394 |
| Start | 123359639:123359639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1204A>G |
| AA Mutation | p.Lys402Glu(p.K402E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287394 |
| Start | 123349352:123349352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1739T>C |
| AA Mutation | p.Ile580Thr(p.I580T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287394 |
| Start | 123322982:123322982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4087A>G |
| AA Mutation | p.Ile1363Val(p.I1363V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287394 |
| Start | 123369935:123369935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.817G>C |
| AA Mutation | p.Asp273His(p.D273H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000287394 |
| Start | 123349430:123349430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1661C>T |
| AA Mutation | p.Thr554Ile(p.T554I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000287394 |
| Start | 123396328:123396328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760726039 |
| CDS Mutation | c.30G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000287394 |
| Start | 123359641:123359642(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1201_1202insGACGATGATGATGATGATGATGATGATGAAGATGATGAAG |
| AA Mutation | p.Tyr401Ter(p.Y401*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000287394 |
| Start | 123328514:123328515(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3543_3544insCTTTGCAAATATTTTCTCCCACTCTGTGGCTTGACTTCTCAAACAC |
| AA Mutation | p.Lys1182LeufsTer23(p.K1182Lfs*23) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000287394 |
| Start | 123370992:123370992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.640-2A>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |