Primary Site >> Stomach Cancer
Gene >> LOXL4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260702 |
| Start | 98258046:98258046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1040T>C |
| AA Mutation | p.Val347Ala(p.V347A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260702 |
| Start | 98257993:98257993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756712441 |
| CDS Mutation | c.1093C>T |
| AA Mutation | p.Arg365Trp(p.R365W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260702 |
| Start | 98259214:98259214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189527571 |
| CDS Mutation | c.716C>T |
| AA Mutation | p.Thr239Met(p.T239M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260702 |
| Start | 98253598:98253598(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372637990 |
| CDS Mutation | c.1790G>A |
| AA Mutation | p.Arg597His(p.R597H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260702 |
| Start | 98262832:98262832(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.188C>T |
| AA Mutation | p.Ala63Val(p.A63V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260702 |
| Start | 98262210:98262210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.281C>T |
| AA Mutation | p.Pro94Leu(p.P94L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000260702 |
| Start | 98252359:98252359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1945C>T |
| AA Mutation | p.Pro649Ser(p.P649S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260702 |
| Start | 98259180:98259180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.750C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260702 |
| Start | 98258045:98258045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112540326 |
| CDS Mutation | c.1041C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260702 |
| Start | 98256807:98256807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1401C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260702 |
| Start | 98258159:98258159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749176974 |
| CDS Mutation | c.927G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000260702 |
| Start | 98262122:98262122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.369T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000260702 |
| Start | 98262088:98262088(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.403delC |
| AA Mutation | p.Arg135GlyfsTer40(p.R135Gfs*40) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000260702 |
| Start | 98256818:98256818(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555163440 |
| CDS Mutation | c.1390C>T |
| AA Mutation | p.Arg464Ter(p.R464*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |