Primary Site >> Stomach Cancer
Gene >> SCARB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000415380 |
| Start | 124810187:124810187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.829C>T |
| AA Mutation | p.Pro277Ser(p.P277S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000415380 |
| Start | 124810278:124810278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.738G>T |
| AA Mutation | p.Trp246Cys(p.W246C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000415380 |
| Start | 124807818:124807818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759465275 |
| CDS Mutation | c.952G>A |
| AA Mutation | p.Glu318Lys(p.E318K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000415380 |
| Start | 124814272:124814272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.560T>C |
| AA Mutation | p.Leu187Pro(p.L187P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000415380 |
| Start | 124810277:124810277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.739C>T |
| AA Mutation | p.His247Tyr(p.H247Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000415380 |
| Start | 124795206:124795206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115774142 |
| CDS Mutation | c.1191C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |