Primary Site >> Stomach Cancer
Gene >> SH3GL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269886 |
| Start | 4366972:4366972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.68G>T |
| AA Mutation | p.Gly23Val(p.G23V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269886 |
| Start | 4363853:4363853(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.491G>A |
| AA Mutation | p.Arg164His(p.R164H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000269886 |
| Start | 4364215:4364215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.338C>T |
| AA Mutation | p.Ala113Val(p.A113V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000269886 |
| Start | 4361690:4361690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367904112 |
| CDS Mutation | c.1017C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000269886 |
| Start | 4361741:4361741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373251765 |
| CDS Mutation | c.966C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000269886 |
| Start | 4365546:4365546(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373649255 |
| CDS Mutation | c.267G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |