Primary Site >> Liver Cancer
Gene >> KANK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711564:711564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.798G>T |
| AA Mutation | p.Gln266His(p.Q266H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 713298:713298(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2532C>A |
| AA Mutation | p.Asn844Lys(p.N844K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 730216:730216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2864T>A |
| AA Mutation | p.Leu955Gln(p.L955Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711084:711084(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.318C>A |
| AA Mutation | p.Phe106Leu(p.F106L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 738429:738429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374492770 |
| CDS Mutation | c.3478G>A |
| AA Mutation | p.Gly1160Ser(p.G1160S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000382297 |
| Start | 740792:740792(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3554A>G |
| AA Mutation | p.Asp1185Gly(p.D1185G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711611:711611(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752429506 |
| CDS Mutation | c.845G>A |
| AA Mutation | p.Arg282Gln(p.R282Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 713335:713335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2569T>G |
| AA Mutation | p.Ser857Ala(p.S857A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382297 |
| Start | 711598:711598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.832G>C |
| AA Mutation | p.Glu278Gln(p.E278Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |