Primary Site >> Stomach Cancer
Gene >> DNTT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371174 |
| Start | 96328739:96328739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1022G>T |
| AA Mutation | p.Gly341Val(p.G341V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371174 |
| Start | 96332564:96332564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1327G>A |
| AA Mutation | p.Ala443Thr(p.A443T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371174 |
| Start | 96327524:96327524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749994764 |
| CDS Mutation | c.931G>A |
| AA Mutation | p.Val311Ile(p.V311I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371174 |
| Start | 96318473:96318473(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.325G>A |
| AA Mutation | p.Glu109Lys(p.E109K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000371174 |
| Start | 96319344:96319344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.461C>T |
| AA Mutation | p.Ala154Val(p.A154V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371174 |
| Start | 96319303:96319303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201827729 |
| CDS Mutation | c.420G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371174 |
| Start | 96327523:96327523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571930329 |
| CDS Mutation | c.930C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000371174 |
| Start | 96304515:96304515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774258749 |
| CDS Mutation | c.18G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |