Primary Site >> Stomach Cancer
Gene >> CCR7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246657 |
| Start | 40554975:40554975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.904A>G |
| AA Mutation | p.Lys302Glu(p.K302E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246657 |
| Start | 40555784:40555784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.95A>G |
| AA Mutation | p.Tyr32Cys(p.Y32C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246657 |
| Start | 40555495:40555495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.384T>G |
| AA Mutation | p.Phe128Leu(p.F128L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246657 |
| Start | 40554768:40554768(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1111G>A |
| AA Mutation | p.Glu371Lys(p.E371K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246657 |
| Start | 40555455:40555455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.424A>G |
| AA Mutation | p.Ser142Gly(p.S142G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246657 |
| Start | 40555137:40555137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568161538 |
| CDS Mutation | c.742C>T |
| AA Mutation | p.Arg248Cys(p.R248C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246657 |
| Start | 40554955:40554955(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs116263918 |
| CDS Mutation | c.924C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |