Primary Site >> Stomach Cancer
Gene >> PASK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241126756:241126756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767264831 |
| CDS Mutation | c.2159C>T |
| AA Mutation | p.Thr720Met(p.T720M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241127356:241127356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776733626 |
| CDS Mutation | c.1559T>C |
| AA Mutation | p.Val520Ala(p.V520A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241139914:241139914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.571G>T |
| AA Mutation | p.Gly191Cys(p.G191C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241126202:241126202(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146183956 |
| CDS Mutation | c.2713C>T |
| AA Mutation | p.Arg905Trp(p.R905W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241140645:241140645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372983773 |
| CDS Mutation | c.305G>A |
| AA Mutation | p.Arg102Gln(p.R102Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241126277:241126277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373048417 |
| CDS Mutation | c.2638C>T |
| AA Mutation | p.Arg880Cys(p.R880C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241126658:241126658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2257G>T |
| AA Mutation | p.Asp753Tyr(p.D753Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241140663:241140663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778811482 |
| CDS Mutation | c.287C>T |
| AA Mutation | p.Thr96Met(p.T96M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000234040 |
| Start | 241137005:241137005(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1136A>C |
| AA Mutation | p.Lys379Thr(p.K379T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241127222:241127222(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1693T>C |
| AA Mutation | p.Cys565Arg(p.C565R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241127225:241127225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1690A>C |
| AA Mutation | p.Met564Leu(p.M564L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241106658:241106658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3880G>A |
| AA Mutation | p.Ala1294Thr(p.A1294T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241112415:241112415(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3358C>T |
| AA Mutation | p.Arg1120Cys(p.R1120C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241137179:241137179(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.962G>A |
| AA Mutation | p.Ser321Asn(p.S321N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241112265:241112265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3508G>A |
| AA Mutation | p.Ala1170Thr(p.A1170T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000234040 |
| Start | 241127377:241127377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1538C>T |
| AA Mutation | p.Ala513Val(p.A513V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241126944:241126944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1971G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241126584:241126584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139322342 |
| CDS Mutation | c.2331C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241126275:241126275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773983757 |
| CDS Mutation | c.2640C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241127259:241127259(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1656A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241126932:241126932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1983G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241127229:241127229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1686T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241143027:241143027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241126302:241126302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2613C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241140590:241140590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.360A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241135890:241135890(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1287C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000234040 |
| Start | 241137995:241137995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765783728 |
| CDS Mutation | c.834C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000234040 |
| Start | 241106639:241106639(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3899delG |
| AA Mutation | p.Gly1300AlafsTer22(p.G1300Afs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000234040 |
| Start | 241122864:241122864(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2940delC |
| AA Mutation | p.Lys981ArgfsTer22(p.K981Rfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000234040 |
| Start | 241127104:241127104(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs773028205 |
| CDS Mutation | c.1811delG |
| AA Mutation | p.Gly604AlafsTer4(p.G604Afs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000234040 |
| Start | 241126484:241126484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776234374 |
| CDS Mutation | c.2431C>T |
| AA Mutation | p.Arg811Ter(p.R811*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |