Primary Site >> Stomach Cancer
Gene >> GDI2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380191 |
| Start | 5768261:5768261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.943A>G |
| AA Mutation | p.Asn315Asp(p.N315D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380191 |
| Start | 5785940:5785940(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201917946 |
| CDS Mutation | c.499A>G |
| AA Mutation | p.Thr167Ala(p.T167A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380191 |
| Start | 5768339:5768339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.865G>T |
| AA Mutation | p.Asp289Tyr(p.D289Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380191 |
| Start | 5786027:5786027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.412C>T |
| AA Mutation | p.Arg138Cys(p.R138C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380191 |
| Start | 5766148:5766148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1196T>G |
| AA Mutation | p.Phe399Cys(p.F399C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380191 |
| Start | 5766584:5766584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1046A>G |
| AA Mutation | p.Tyr349Cys(p.Y349C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380191 |
| Start | 5766631:5766631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774905963 |
| CDS Mutation | c.999C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |