Primary Site >> Stomach Cancer
Gene >> ZNF331
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253144 |
| Start | 53577237:53577237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.677G>A |
| AA Mutation | p.Arg226His(p.R226H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253144 |
| Start | 53576944:53576944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.384G>T |
| AA Mutation | p.Glu128Asp(p.E128D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253144 |
| Start | 53576823:53576823(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.263C>T |
| AA Mutation | p.Thr88Met(p.T88M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253144 |
| Start | 53576723:53576723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.163A>C |
| AA Mutation | p.Ser55Arg(p.S55R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253144 |
| Start | 53577153:53577153(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.593G>T |
| AA Mutation | p.Trp198Leu(p.W198L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253144 |
| Start | 53577741:53577741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1181A>G |
| AA Mutation | p.Tyr394Cys(p.Y394C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253144 |
| Start | 53577572:53577572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1012T>G |
| AA Mutation | p.Trp338Gly(p.W338G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253144 |
| Start | 53576885:53576885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.325A>G |
| AA Mutation | p.Lys109Glu(p.K109E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253144 |
| Start | 53577414:53577414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.854G>A |
| AA Mutation | p.Ser285Asn(p.S285N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253144 |
| Start | 53577877:53577877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144369706 |
| CDS Mutation | c.1317C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253144 |
| Start | 53577748:53577748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199753274 |
| CDS Mutation | c.1188G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |