Primary Site >> Liver Cancer
Gene >> WNK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93288839:93288839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4196T>A |
| AA Mutation | p.Leu1399Gln(p.L1399Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93256363:93256363(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2099C>A |
| AA Mutation | p.Pro700Gln(p.P700Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93229811:93229811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.797A>T |
| AA Mutation | p.Lys266Met(p.K266M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93268884:93268884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769311608 |
| CDS Mutation | c.4078G>A |
| AA Mutation | p.Ala1360Thr(p.A1360T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93261899:93261899(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370654793 |
| CDS Mutation | c.3152C>T |
| AA Mutation | p.Ser1051Leu(p.S1051L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93317975:93317975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6842G>T |
| AA Mutation | p.Arg2281Leu(p.R2281L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93289556:93289556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4913A>G |
| AA Mutation | p.Asp1638Gly(p.D1638G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297954 |
| Start | 93299114:93299114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6079G>A |
| AA Mutation | p.Ala2027Thr(p.A2027T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93292514:93292514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5160T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93259323:93259323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2775T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93308513:93308513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6556C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297954 |
| Start | 93317567:93317567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756768259 |
| CDS Mutation | c.6675G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |