Primary Site >> Stomach Cancer
Gene >> CX3CL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006053 |
| Start | 57382653:57382653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201467674 |
| CDS Mutation | c.815C>T |
| AA Mutation | p.Thr272Met(p.T272M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006053 |
| Start | 57382331:57382331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.493T>C |
| AA Mutation | p.Ser165Pro(p.S165P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006053 |
| Start | 57382386:57382386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771801757 |
| CDS Mutation | c.548C>T |
| AA Mutation | p.Thr183Met(p.T183M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006053 |
| Start | 57379744:57379744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.181C>T |
| AA Mutation | p.Arg61Cys(p.R61C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006053 |
| Start | 57382992:57382992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199662906 |
| CDS Mutation | c.1154G>A |
| AA Mutation | p.Arg385Gln(p.R385Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006053 |
| Start | 57382319:57382319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138964688 |
| CDS Mutation | c.481G>A |
| AA Mutation | p.Val161Met(p.V161M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000006053 |
| Start | 57382865:57382865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762102080 |
| CDS Mutation | c.1027G>A |
| AA Mutation | p.Val343Met(p.V343M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000006053 |
| Start | 57382193:57382193(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.359delG |
| AA Mutation | p.Gly120GlufsTer42(p.G120Efs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000006053 |
| Start | 57382344:57382345(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.512dupC |
| AA Mutation | p.Thr172AspfsTer41(p.T172Dfs*41) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |