Primary Site >> Stomach Cancer
Gene >> ALOX5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45443137:45443137(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1372C>T |
| AA Mutation | p.Arg458Trp(p.R458W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45445616:45445616(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151270582 |
| CDS Mutation | c.1954C>T |
| AA Mutation | p.Arg652Cys(p.R652C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45443065:45443065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs554154845 |
| CDS Mutation | c.1300G>A |
| AA Mutation | p.Val434Met(p.V434M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45382651:45382651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.319G>A |
| AA Mutation | p.Asp107Asn(p.D107N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45412286:45412286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.527T>C |
| AA Mutation | p.Val176Ala(p.V176A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45395902:45395902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs187523060 |
| CDS Mutation | c.397C>T |
| AA Mutation | p.Arg133Cys(p.R133C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45443525:45443525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766026494 |
| CDS Mutation | c.1561C>T |
| AA Mutation | p.Arg521Cys(p.R521C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45382543:45382543(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.211G>A |
| AA Mutation | p.Glu71Lys(p.E71K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45382580:45382580(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.248T>C |
| AA Mutation | p.Leu83Pro(p.L83P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374391 |
| Start | 45445662:45445662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758477278 |
| CDS Mutation | c.2000G>A |
| AA Mutation | p.Arg667Gln(p.R667Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374391 |
| Start | 45443512:45443512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1548C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374391 |
| Start | 45443524:45443524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1560C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374391 |
| Start | 45443172:45443172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1407C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374391 |
| Start | 45443187:45443187(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543892108 |
| CDS Mutation | c.1422C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |