Primary Site >> Stomach Cancer
Gene >> LOXL3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264094 |
| Start | 74535605:74535605(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1399G>A |
| AA Mutation | p.Ala467Thr(p.A467T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264094 |
| Start | 74549507:74549507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.554C>T |
| AA Mutation | p.Thr185Met(p.T185M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264094 |
| Start | 74534601:74534601(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1753C>A |
| AA Mutation | p.His585Asn(p.H585N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264094 |
| Start | 74534338:74534338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769903746 |
| CDS Mutation | c.1917C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264094 |
| Start | 74552404:74552404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.231G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264094 |
| Start | 74534635:74534635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1719T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264094 |
| Start | 74536125:74536125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1119A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264094 |
| Start | 74550218:74550218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760639330 |
| CDS Mutation | c.444C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264094 |
| Start | 74552580:74552580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768888102 |
| CDS Mutation | c.55C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |