Primary Site >> Stomach Cancer
Gene >> HSPA9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297185 |
| Start | 138566666:138566666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932C>G |
| AA Mutation | p.Ala311Gly(p.A311G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297185 |
| Start | 138557974:138557974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752447855 |
| CDS Mutation | c.1528C>T |
| AA Mutation | p.Pro510Ser(p.P510S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000297185 |
| Start | 138559887:138559887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1387A>G |
| AA Mutation | p.Thr463Ala(p.T463A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297185 |
| Start | 138556470:138556470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148730345 |
| CDS Mutation | c.1944C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297185 |
| Start | 138567658:138567658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762248139 |
| CDS Mutation | c.600G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000297185 |
| Start | 138558628:138558628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149852902 |
| CDS Mutation | c.1440G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |