Primary Site >> Stomach Cancer
Gene >> SLAMF7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368043 |
| Start | 160750373:160750373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.719T>G |
| AA Mutation | p.Leu240Arg(p.L240R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368043 |
| Start | 160751422:160751422(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.847G>C |
| AA Mutation | p.Glu283Gln(p.E283Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368043 |
| Start | 160750393:160750393(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746119808 |
| CDS Mutation | c.739C>A |
| AA Mutation | p.Leu247Ile(p.L247I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368043 |
| Start | 160748352:160748352(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.214G>T |
| AA Mutation | p.Val72Leu(p.V72L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368043 |
| Start | 160748397:160748397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.259G>T |
| AA Mutation | p.Gly87Cys(p.G87C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368043 |
| Start | 160748249:160748249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.111G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368043 |
| Start | 160752236:160752236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.924A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368043 |
| Start | 160748228:160748228(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766493799 |
| CDS Mutation | c.90C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000368043 |
| Start | 160751344:160751344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.770-1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |