Primary Site >> Stomach Cancer
Gene >> CXCR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318507 |
| Start | 218135360:218135360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199777583 |
| CDS Mutation | c.559G>A |
| AA Mutation | p.Val187Ile(p.V187I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318507 |
| Start | 218135094:218135094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.293C>T |
| AA Mutation | p.Ala98Val(p.A98V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318507 |
| Start | 218135508:218135508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144013681 |
| CDS Mutation | c.707G>A |
| AA Mutation | p.Arg236His(p.R236H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318507 |
| Start | 218134858:218134858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.57T>A |
| AA Mutation | p.Asp19Glu(p.D19E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318507 |
| Start | 218135290:218135290(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.489A>C |
| AA Mutation | p.Lys163Asn(p.K163N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318507 |
| Start | 218135223:218135223(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.422G>A |
| AA Mutation | p.Ser141Asn(p.S141N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318507 |
| Start | 218135117:218135117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.316G>A |
| AA Mutation | p.Ala106Thr(p.A106T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000318507 |
| Start | 218134910:218134910(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs75759064 |
| CDS Mutation | c.109G>A |
| AA Mutation | p.Ala37Thr(p.A37T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000318507 |
| Start | 218134909:218134909(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201373363 |
| CDS Mutation | c.108C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |