Primary Site >> Stomach Cancer
Gene >> HMOX1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216117 |
| Start | 35389936:35389936(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145427664 |
| CDS Mutation | c.709C>T |
| AA Mutation | p.Arg237Cys(p.R237C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216117 |
| Start | 35386839:35386839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747303322 |
| CDS Mutation | c.299G>A |
| AA Mutation | p.Arg100His(p.R100H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216117 |
| Start | 35387058:35387058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.518C>T |
| AA Mutation | p.Ala173Val(p.A173V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216117 |
| Start | 35387062:35387062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.522T>A |
| AA Mutation | p.Ser174Arg(p.S174R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216117 |
| Start | 35393516:35393516(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.785G>A |
| AA Mutation | p.Arg262His(p.R262H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000216117 |
| Start | 35389942:35389942(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374813554 |
| CDS Mutation | c.715C>T |
| AA Mutation | p.Arg239Trp(p.R239W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |