Primary Site >> Stomach Cancer
Gene >> LMO3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320122 |
| Start | 16600710:16600710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.151G>T |
| AA Mutation | p.Gly51Cys(p.G51C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320122 |
| Start | 16560472:16560472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.273G>A |
| AA Mutation | p.Met91Ile(p.M91I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320122 |
| Start | 16600814:16600814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.47G>A |
| AA Mutation | p.Cys16Tyr(p.C16Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000320122 |
| Start | 16600808:16600808(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754453605 |
| CDS Mutation | c.53G>A |
| AA Mutation | p.Arg18Gln(p.R18Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320122 |
| Start | 16560514:16560514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149014326 |
| CDS Mutation | c.231C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000320122 |
| Start | 16551273:16551273(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543260958 |
| CDS Mutation | c.387G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |