Primary Site >> Stomach Cancer
Gene >> GNAI3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369851 |
| Start | 109548803:109548803(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.83A>G |
| AA Mutation | p.Glu28Gly(p.E28G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369851 |
| Start | 109573927:109573927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.193G>A |
| AA Mutation | p.Glu65Lys(p.E65K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369851 |
| Start | 109582442:109582442(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.467T>C |
| AA Mutation | p.Leu156Pro(p.L156P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369851 |
| Start | 109579295:109579295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758640921 |
| CDS Mutation | c.395G>A |
| AA Mutation | p.Arg132Gln(p.R132Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369851 |
| Start | 109573955:109573955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.221A>G |
| AA Mutation | p.Tyr74Cys(p.Y74C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369851 |
| Start | 109586786:109586786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.778A>G |
| AA Mutation | p.Thr260Ala(p.T260A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369851 |
| Start | 109592083:109592083(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.915C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369851 |
| Start | 109579303:109579303(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.406delG |
| AA Mutation | p.Val136TyrfsTer21(p.V136Yfs*21) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000369851 |
| Start | 109586247:109586247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766202043 |
| CDS Mutation | c.622C>T |
| AA Mutation | p.Arg208Ter(p.R208*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |