Primary Site >> Stomach Cancer
Gene >> ADA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372874 |
| Start | 44620366:44620366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1011A>C |
| AA Mutation | p.Glu337Asp(p.E337D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372874 |
| Start | 44623021:44623021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371353841 |
| CDS Mutation | c.664G>A |
| AA Mutation | p.Glu222Lys(p.E222K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372874 |
| Start | 44626471:44626471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774510141 |
| CDS Mutation | c.347C>A |
| AA Mutation | p.Pro116His(p.P116H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372874 |
| Start | 44621049:44621049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758501653 |
| CDS Mutation | c.944T>C |
| AA Mutation | p.Met315Thr(p.M315T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000372874 |
| Start | 44620325:44620325(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1052A>G |
| AA Mutation | p.Tyr351Cys(p.Y351C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372874 |
| Start | 44621051:44621051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.942C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372874 |
| Start | 44621102:44621102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776360146 |
| CDS Mutation | c.891G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000372874 |
| Start | 44629157:44629157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748611869 |
| CDS Mutation | c.108C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |