Primary Site >> Stomach Cancer
Gene >> GFPT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357308 |
| Start | 69363563:69363563(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201322234 |
| CDS Mutation | c.331C>T |
| AA Mutation | p.Arg111Cys(p.R111C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357308 |
| Start | 69338538:69338538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1231G>C |
| AA Mutation | p.Glu411Gln(p.E411Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357308 |
| Start | 69359275:69359275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.401A>C |
| AA Mutation | p.Lys134Thr(p.K134T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357308 |
| Start | 69350169:69350169(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.754G>A |
| AA Mutation | p.Gly252Arg(p.G252R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357308 |
| Start | 69363562:69363562(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189717232 |
| CDS Mutation | c.332G>A |
| AA Mutation | p.Arg111His(p.R111H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357308 |
| Start | 69342201:69342201(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1154G>A |
| AA Mutation | p.Arg385Gln(p.R385Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000357308 |
| Start | 69354498:69354498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.676T>C |
| AA Mutation | p.Tyr226His(p.Y226H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357308 |
| Start | 69328343:69328343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1821G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000357308 |
| Start | 69342215:69342215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781010273 |
| CDS Mutation | c.1140G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |