Primary Site >> Stomach Cancer
Gene >> SGCZ
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382080 |
| Start | 14102426:14102426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.694T>G |
| AA Mutation | p.Phe232Val(p.F232V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382080 |
| Start | 14090454:14090454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.928C>A |
| AA Mutation | p.Leu310Met(p.L310M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382080 |
| Start | 14090529:14090529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139184216 |
| CDS Mutation | c.853G>A |
| AA Mutation | p.Val285Ile(p.V285I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382080 |
| Start | 14102437:14102437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.683C>T |
| AA Mutation | p.Ala228Val(p.A228V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382080 |
| Start | 14090587:14090587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.795C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382080 |
| Start | 14108195:14108195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775208052 |
| CDS Mutation | c.588G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382080 |
| Start | 14554789:14554789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775777311 |
| CDS Mutation | c.177C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000382080 |
| Start | 14090607:14090607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.775G>T |
| AA Mutation | p.Gly259Ter(p.G259*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |