Primary Site >> Stomach Cancer
Gene >> HADHA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380649 |
| Start | 26191602:26191602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2027G>A |
| AA Mutation | p.Arg676His(p.R676H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380649 |
| Start | 26191263:26191263(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2279A>G |
| AA Mutation | p.Lys760Arg(p.K760R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380649 |
| Start | 26204153:26204153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761474139 |
| CDS Mutation | c.1129G>A |
| AA Mutation | p.Ala377Thr(p.A377T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380649 |
| Start | 26193708:26193708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1754C>G |
| AA Mutation | p.Ala585Gly(p.A585G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380649 |
| Start | 26212591:26212591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.954C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380649 |
| Start | 26204094:26204094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781338540 |
| CDS Mutation | c.1188G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380649 |
| Start | 26191367:26191367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375399631 |
| CDS Mutation | c.2175C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000380649 |
| Start | 26214490:26214490(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137852775 |
| CDS Mutation | c.871C>T |
| AA Mutation | p.Arg291Ter(p.R291*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |