Primary Site >> Stomach Cancer
Gene >> APOH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205948 |
| Start | 66220618:66220618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.540G>A |
| AA Mutation | p.Met180Ile(p.M180I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205948 |
| Start | 66220712:66220712(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113544357 |
| CDS Mutation | c.446C>T |
| AA Mutation | p.Thr149Met(p.T149M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205948 |
| Start | 66214628:66214628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.807A>C |
| AA Mutation | p.Lys269Asn(p.K269N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205948 |
| Start | 66223725:66223725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.388T>C |
| AA Mutation | p.Trp130Arg(p.W130R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000205948 |
| Start | 66228088:66228088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.173G>A |
| AA Mutation | p.Arg58Gln(p.R58Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000205948 |
| Start | 66216843:66216843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777337011 |
| CDS Mutation | c.729G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |