Primary Site >> Stomach Cancer
Gene >> CXCR1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164280:218164280(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932A>C |
| AA Mutation | p.Asn311Thr(p.N311T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164404:218164404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.808A>G |
| AA Mutation | p.Thr270Ala(p.T270A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164532:218164532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140085060 |
| CDS Mutation | c.680G>A |
| AA Mutation | p.Arg227His(p.R227H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164781:218164781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.431G>A |
| AA Mutation | p.Arg144His(p.R144H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164953:218164953(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.259C>A |
| AA Mutation | p.Leu87Ile(p.L87I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164282:218164282(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.930A>C |
| AA Mutation | p.Gln310His(p.Q310H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218165057:218165057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.155T>G |
| AA Mutation | p.Leu52Arg(p.L52R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164224:218164224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.988T>G |
| AA Mutation | p.Phe330Val(p.F330V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164604:218164604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs538588993 |
| CDS Mutation | c.608G>A |
| AA Mutation | p.Arg203Gln(p.R203Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164782:218164782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs111741549 |
| CDS Mutation | c.430C>T |
| AA Mutation | p.Arg144Cys(p.R144C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164492:218164492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.720C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164186:218164186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144791200 |
| CDS Mutation | c.1026G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000295683 |
| Start | 218164570:218164570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752745195 |
| CDS Mutation | c.642G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |