Primary Site >> Stomach Cancer
Gene >> CHST9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581714 |
| Start | 27142702:27142702(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.108A>C |
| AA Mutation | p.Glu36Asp(p.E36D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581714 |
| Start | 27142701:27142701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.109G>A |
| AA Mutation | p.Glu37Lys(p.E37K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581714 |
| Start | 26916465:26916465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1126G>T |
| AA Mutation | p.Asp376Tyr(p.D376Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581714 |
| Start | 26916500:26916500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1091A>G |
| AA Mutation | p.Tyr364Cys(p.Y364C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581714 |
| Start | 27142731:27142731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.79C>T |
| AA Mutation | p.Leu27Phe(p.L27F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000581714 |
| Start | 26917322:26917322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.269T>C |
| AA Mutation | p.Val90Ala(p.V90A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000581714 |
| Start | 27142758:27142758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.52C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000581714 |
| Start | 27142780:27142780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.30C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000581714 |
| Start | 26917024:26917024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764768308 |
| CDS Mutation | c.567C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |