Primary Site >> Stomach Cancer
Gene >> NAPRT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449291 |
| Start | 143576799:143576799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199843319 |
| CDS Mutation | c.728C>T |
| AA Mutation | p.Ala243Val(p.A243V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449291 |
| Start | 143576764:143576764(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.763G>A |
| AA Mutation | p.Ala255Thr(p.A255T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449291 |
| Start | 143576474:143576474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.980A>G |
| AA Mutation | p.Gln327Arg(p.Q327R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000449291 |
| Start | 143575255:143575255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1382A>G |
| AA Mutation | p.Glu461Gly(p.E461G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449291 |
| Start | 143575254:143575254(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1383G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000449291 |
| Start | 143577378:143577378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763763850 |
| CDS Mutation | c.459G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |