Primary Site >> Stomach Cancer
Gene >> MUC7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304887 |
| Start | 70481664:70481664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.920C>G |
| AA Mutation | p.Pro307Arg(p.P307R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000304887 |
| Start | 70480799:70480799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.55T>G |
| AA Mutation | p.Phe19Val(p.F19V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304887 |
| Start | 70481132:70481132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.388A>G |
| AA Mutation | p.Thr130Ala(p.T130A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304887 |
| Start | 70480994:70480994(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.250T>G |
| AA Mutation | p.Phe84Val(p.F84V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304887 |
| Start | 70481267:70481267(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.523A>G |
| AA Mutation | p.Thr175Ala(p.T175A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304887 |
| Start | 70480914:70480914(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764963529 |
| CDS Mutation | c.170C>T |
| AA Mutation | p.Pro57Leu(p.P57L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |