Primary Site >> Stomach Cancer
Gene >> TAOK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29979025:29979025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.404C>T |
| AA Mutation | p.Ala135Val(p.A135V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29986370:29986370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777936445 |
| CDS Mutation | c.2098C>T |
| AA Mutation | p.Arg700Cys(p.R700C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29985250:29985250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1460C>T |
| AA Mutation | p.Ala487Val(p.A487V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29985559:29985559(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770907647 |
| CDS Mutation | c.1769G>A |
| AA Mutation | p.Arg590His(p.R590H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29986548:29986548(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2276C>A |
| AA Mutation | p.Pro759His(p.P759H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29987491:29987491(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3219G>T |
| AA Mutation | p.Gln1073His(p.Q1073H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29983656:29983656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1414G>A |
| AA Mutation | p.Ala472Thr(p.A472T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29987699:29987699(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3427C>A |
| AA Mutation | p.Pro1143Thr(p.P1143T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29979457:29979457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.604T>C |
| AA Mutation | p.Tyr202His(p.Y202H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29978980:29978980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.359A>C |
| AA Mutation | p.Lys120Thr(p.K120T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29986370:29986370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2098C>G |
| AA Mutation | p.Arg700Gly(p.R700G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29982750:29982750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.848G>A |
| AA Mutation | p.Arg283Gln(p.R283Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29986607:29986607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2335G>T |
| AA Mutation | p.Gly779Cys(p.G779C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29987709:29987709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3437T>C |
| AA Mutation | p.Leu1146Pro(p.L1146P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29986991:29986991(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2719G>A |
| AA Mutation | p.Glu907Lys(p.E907K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29985474:29985474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371473286 |
| CDS Mutation | c.1684C>T |
| AA Mutation | p.Arg562Trp(p.R562W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29982853:29982853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.951C>A |
| AA Mutation | p.Phe317Leu(p.F317L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29985811:29985811(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758342146 |
| CDS Mutation | c.1942C>T |
| AA Mutation | p.Arg648Cys(p.R648C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000308893 |
| Start | 29987685:29987685(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3413G>A |
| AA Mutation | p.Arg1138His(p.R1138H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308893 |
| Start | 29978106:29978106(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.150T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000308893 |
| Start | 29987794:29987794(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369839391 |
| CDS Mutation | c.3522G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |