Primary Site >> Stomach Cancer
Gene >> AMACR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335606 |
| Start | 33989116:33989116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1126A>G |
| AA Mutation | p.Asn376Asp(p.N376D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335606 |
| Start | 34004614:34004614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770694101 |
| CDS Mutation | c.512G>A |
| AA Mutation | p.Arg171His(p.R171H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335606 |
| Start | 34005859:34005859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.288G>C |
| AA Mutation | p.Gln96His(p.Q96H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335606 |
| Start | 34005795:34005795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763403225 |
| CDS Mutation | c.352C>T |
| AA Mutation | p.Arg118Trp(p.R118W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335606 |
| Start | 34007965:34007965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.55T>C |
| AA Mutation | p.Phe19Leu(p.F19L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335606 |
| Start | 34004697:34004697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368427062 |
| CDS Mutation | c.429G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |