Primary Site >> Stomach Cancer
Gene >> NAGLU
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225927 |
| Start | 42541018:42541018(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775364669 |
| CDS Mutation | c.833C>T |
| AA Mutation | p.Ser278Phe(p.S278F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225927 |
| Start | 42543793:42543793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1787G>A |
| AA Mutation | p.Gly596Asp(p.G596D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225927 |
| Start | 42538701:42538701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775646404 |
| CDS Mutation | c.710G>A |
| AA Mutation | p.Gly237Asp(p.G237D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225927 |
| Start | 42538674:42538674(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146456266 |
| CDS Mutation | c.683G>A |
| AA Mutation | p.Arg228Gln(p.R228Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225927 |
| Start | 42537441:42537441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.427G>A |
| AA Mutation | p.Val143Met(p.V143M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000225927 |
| Start | 42538397:42538397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.590C>T |
| AA Mutation | p.Ala197Val(p.A197V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000225927 |
| Start | 42543329:42543329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751479777 |
| CDS Mutation | c.1323G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |