Primary Site >> Stomach Cancer
Gene >> OR2D2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299459 |
| Start | 6892173:6892173(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.328A>G |
| AA Mutation | p.Thr110Ala(p.T110A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299459 |
| Start | 6892110:6892110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs574075868 |
| CDS Mutation | c.391C>T |
| AA Mutation | p.Arg131Cys(p.R131C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299459 |
| Start | 6891810:6891810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.691A>C |
| AA Mutation | p.Thr231Pro(p.T231P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299459 |
| Start | 6891689:6891689(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.812C>G |
| AA Mutation | p.Ser271Trp(p.S271W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299459 |
| Start | 6892164:6892164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147307045 |
| CDS Mutation | c.337G>A |
| AA Mutation | p.Ala113Thr(p.A113T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299459 |
| Start | 6892401:6892401(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.100G>A |
| AA Mutation | p.Val34Ile(p.V34I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299459 |
| Start | 6892116:6892116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.385C>T |
| AA Mutation | p.Pro129Ser(p.P129S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299459 |
| Start | 6892413:6892413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113796560 |
| CDS Mutation | c.88G>A |
| AA Mutation | p.Val30Ile(p.V30I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000299459 |
| Start | 6892339:6892339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766531079 |
| CDS Mutation | c.162A>C |
| AA Mutation | p.Gln54His(p.Q54H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000299459 |
| Start | 6892165:6892165(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140944764 |
| CDS Mutation | c.336C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |