Primary Site >> Stomach Cancer
Gene >> PCK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24103602:24103602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146891790 |
| CDS Mutation | c.1561C>T |
| AA Mutation | p.Arg521Cys(p.R521C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24103216:24103216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61737097 |
| CDS Mutation | c.1429G>A |
| AA Mutation | p.Ala477Thr(p.A477T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24097043:24097043(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.181C>T |
| AA Mutation | p.His61Tyr(p.H61Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24098580:24098580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755045133 |
| CDS Mutation | c.566G>A |
| AA Mutation | p.Arg189His(p.R189H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24100003:24100003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750677484 |
| CDS Mutation | c.1024C>T |
| AA Mutation | p.Arg342Trp(p.R342W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24099648:24099648(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781084380 |
| CDS Mutation | c.943C>T |
| AA Mutation | p.Arg315Trp(p.R315W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24103620:24103620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1579C>T |
| AA Mutation | p.Pro527Ser(p.P527S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24103193:24103193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201340475 |
| CDS Mutation | c.1406G>A |
| AA Mutation | p.Arg469His(p.R469H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24100144:24100144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1165G>A |
| AA Mutation | p.Glu389Lys(p.E389K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24102860:24102860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551184706 |
| CDS Mutation | c.1342G>A |
| AA Mutation | p.Ala448Thr(p.A448T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216780 |
| Start | 24103542:24103542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199570303 |
| CDS Mutation | c.1501C>T |
| AA Mutation | p.Arg501Trp(p.R501W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216780 |
| Start | 24099650:24099650(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749278970 |
| CDS Mutation | c.945G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216780 |
| Start | 24103526:24103526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200462967 |
| CDS Mutation | c.1485C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216780 |
| Start | 24103754:24103754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1713A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216780 |
| Start | 24097105:24097105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.243C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000216780 |
| Start | 24098254:24098254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764682284 |
| CDS Mutation | c.327G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000216780 |
| Start | 24098268:24098270(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs751483556 |
| CDS Mutation | c.343_345delTCT |
| AA Mutation | p.Ser115del(p.S115del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |