Primary Site >> Stomach Cancer
Gene >> LCK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336890 |
| Start | 32279740:32279740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1034C>T |
| AA Mutation | p.Ala345Val(p.A345V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336890 |
| Start | 32275366:32275366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.324A>T |
| AA Mutation | p.Glu108Asp(p.E108D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336890 |
| Start | 32274764:32274764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139649211 |
| CDS Mutation | c.133C>T |
| AA Mutation | p.Arg45Trp(p.R45W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336890 |
| Start | 32276705:32276705(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.883C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336890 |
| Start | 32279975:32279975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779398676 |
| CDS Mutation | c.1176C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336890 |
| Start | 32275006:32275006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.201C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |