Primary Site >> Stomach Cancer
Gene >> ADORA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309502 |
| Start | 203165791:203165791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766823930 |
| CDS Mutation | c.872G>A |
| AA Mutation | p.Arg291His(p.R291H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309502 |
| Start | 203128946:203128946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.105G>T |
| AA Mutation | p.Lys35Asn(p.K35N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309502 |
| Start | 203165727:203165727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.808A>C |
| AA Mutation | p.Thr270Pro(p.T270P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309502 |
| Start | 203128986:203128986(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.145G>A |
| AA Mutation | p.Val49Met(p.V49M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000309502 |
| Start | 203128888:203128888(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.47A>G |
| AA Mutation | p.Glu16Gly(p.E16G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309502 |
| Start | 203129042:203129042(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.201C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309502 |
| Start | 203165294:203165294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs562367584 |
| CDS Mutation | c.375G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309502 |
| Start | 203165399:203165399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.480C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309502 |
| Start | 203165585:203165585(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201849915 |
| CDS Mutation | c.666G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000309502 |
| Start | 203128847:203128847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61731145 |
| CDS Mutation | c.6G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |