Primary Site >> Stomach Cancer
Gene >> PCK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319441 |
| Start | 57562129:57562129(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536299130 |
| CDS Mutation | c.283G>A |
| AA Mutation | p.Val95Ile(p.V95I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319441 |
| Start | 57563721:57563721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747438321 |
| CDS Mutation | c.955G>A |
| AA Mutation | p.Ala319Thr(p.A319T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319441 |
| Start | 57565394:57565394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1459G>T |
| AA Mutation | p.Gly487Cys(p.G487C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319441 |
| Start | 57561446:57561446(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs548898026 |
| CDS Mutation | c.35C>T |
| AA Mutation | p.Ser12Leu(p.S12L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319441 |
| Start | 57564291:57564291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368785323 |
| CDS Mutation | c.1084G>A |
| AA Mutation | p.Glu362Lys(p.E362K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319441 |
| Start | 57563608:57563608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200991428 |
| CDS Mutation | c.842C>T |
| AA Mutation | p.Ala281Val(p.A281V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319441 |
| Start | 57563625:57563625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747837917 |
| CDS Mutation | c.859G>A |
| AA Mutation | p.Ala287Thr(p.A287T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000319441 |
| Start | 57565759:57565760(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1833_1834dupGA |
| AA Mutation | p.Ile612ArgfsTer5(p.I612Rfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |