Primary Site >> Stomach Cancer
Gene >> LOXL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23341143:23341143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.592C>T |
| AA Mutation | p.Arg198Cys(p.R198C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23341142:23341142(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369286803 |
| CDS Mutation | c.593G>A |
| AA Mutation | p.Arg198His(p.R198H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23341119:23341119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140591037 |
| CDS Mutation | c.616G>A |
| AA Mutation | p.Val206Met(p.V206M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23302091:23302091(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752408071 |
| CDS Mutation | c.2069G>A |
| AA Mutation | p.Arg690His(p.R690H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23298108:23298108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765016338 |
| CDS Mutation | c.2260G>A |
| AA Mutation | p.Glu754Lys(p.E754K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23309797:23309797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1751C>T |
| AA Mutation | p.Ala584Val(p.A584V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23319928:23319928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1427T>C |
| AA Mutation | p.Val476Ala(p.V476A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23341011:23341011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761495594 |
| CDS Mutation | c.724T>C |
| AA Mutation | p.Tyr242His(p.Y242H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23341050:23341050(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769934464 |
| CDS Mutation | c.685G>A |
| AA Mutation | p.Val229Met(p.V229M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23309852:23309852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766054276 |
| CDS Mutation | c.1696C>T |
| AA Mutation | p.Arg566Trp(p.R566W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389131 |
| Start | 23333421:23333421(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754340605 |
| CDS Mutation | c.946C>T |
| AA Mutation | p.Arg316Trp(p.R316W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23302054:23302054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546152513 |
| CDS Mutation | c.2106C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23328485:23328485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1047C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23333512:23333512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.855C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23333437:23333437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747695442 |
| CDS Mutation | c.930C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23328479:23328479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777151562 |
| CDS Mutation | c.1053C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23302132:23302132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779774774 |
| CDS Mutation | c.2028C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23298103:23298103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2265G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23328455:23328455(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367771495 |
| CDS Mutation | c.1077G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23316995:23316995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748190912 |
| CDS Mutation | c.1590C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389131 |
| Start | 23317013:23317013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142665521 |
| CDS Mutation | c.1572C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |