Primary Site >> Stomach Cancer
Gene >> LNX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263925 |
| Start | 53476952:53476952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1693G>A |
| AA Mutation | p.Glu565Lys(p.E565K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263925 |
| Start | 53573776:53573776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.227C>T |
| AA Mutation | p.Pro76Leu(p.P76L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263925 |
| Start | 53498653:53498653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.966C>A |
| AA Mutation | p.Asp322Glu(p.D322E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263925 |
| Start | 53496349:53496349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201792197 |
| CDS Mutation | c.1024C>T |
| AA Mutation | p.Arg342Cys(p.R342C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000263925 |
| Start | 53507412:53507412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147992678 |
| CDS Mutation | c.680C>T |
| AA Mutation | p.Ala227Val(p.A227V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263925 |
| Start | 53496389:53496389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752450046 |
| CDS Mutation | c.984C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263925 |
| Start | 53460982:53460982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2112C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000263925 |
| Start | 53498737:53498737(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138813024 |
| CDS Mutation | c.882C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |