Primary Site >> Stomach Cancer
Gene >> SNX9
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392185 |
| Start | 157938661:157938661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1562A>G |
| AA Mutation | p.Asp521Gly(p.D521G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392185 |
| Start | 157928607:157928607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1193A>C |
| AA Mutation | p.Lys398Thr(p.K398T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392185 |
| Start | 157875102:157875102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.226G>A |
| AA Mutation | p.Asp76Asn(p.D76N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000392185 |
| Start | 157921651:157921651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1070G>T |
| AA Mutation | p.Arg357Leu(p.R357L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392185 |
| Start | 157909967:157909967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.891C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392185 |
| Start | 157875059:157875059(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.183C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000392185 |
| Start | 157875155:157875155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750073691 |
| CDS Mutation | c.279G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |