Primary Site >> Stomach Cancer
Gene >> CXCR5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292174 |
| Start | 118894146:118894146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762687395 |
| CDS Mutation | c.602G>A |
| AA Mutation | p.Arg201His(p.R201H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292174 |
| Start | 118894398:118894398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373222312 |
| CDS Mutation | c.854C>T |
| AA Mutation | p.Ala285Val(p.A285V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292174 |
| Start | 118894295:118894295(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751C>T |
| AA Mutation | p.Arg251Cys(p.R251C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000292174 |
| Start | 118894652:118894652(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1108A>T |
| AA Mutation | p.Thr370Ser(p.T370S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292174 |
| Start | 118894291:118894291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.747G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292174 |
| Start | 118893802:118893802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.258G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292174 |
| Start | 118894375:118894375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.831C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292174 |
| Start | 118894546:118894546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147267963 |
| CDS Mutation | c.1002G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000292174 |
| Start | 118894021:118894021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.477C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000292174 |
| Start | 118893670:118893670(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.129delG |
| AA Mutation | p.Leu45SerfsTer22(p.L45Sfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000292174 |
| Start | 118894621:118894624(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs781445622 |
| CDS Mutation | c.1080_1083delCTCT |
| AA Mutation | p.Glu362GlnfsTer39(p.E362Qfs*39) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |