Primary Site >> Stomach Cancer
Gene >> DGCR8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20107361:20107361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2087G>A |
| AA Mutation | p.Arg696His(p.R696H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20106669:20106669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1967C>A |
| AA Mutation | p.Ala656Glu(p.A656E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20086408:20086408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.445G>T |
| AA Mutation | p.Gly149Cys(p.G149C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20091943:20091943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1579C>T |
| AA Mutation | p.Arg527Cys(p.R527C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20091593:20091593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1465C>A |
| AA Mutation | p.Leu489Ile(p.L489I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20086400:20086400(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201293912 |
| CDS Mutation | c.437C>T |
| AA Mutation | p.Ala146Val(p.A146V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20086114:20086114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.151G>A |
| AA Mutation | p.Val51Ile(p.V51I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20091555:20091555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1427C>T |
| AA Mutation | p.Ala476Val(p.A476V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20108997:20108997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2232G>T |
| AA Mutation | p.Glu744Asp(p.E744D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20089672:20089672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759142349 |
| CDS Mutation | c.884G>A |
| AA Mutation | p.Arg295His(p.R295H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000351989 |
| Start | 20086390:20086390(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.427G>A |
| AA Mutation | p.Asp143Asn(p.D143N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000351989 |
| Start | 20110063:20110063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765113050 |
| CDS Mutation | c.2277G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |