Primary Site >> Stomach Cancer
Gene >> SH3GL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380607 |
| Start | 17786465:17786465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545737125 |
| CDS Mutation | c.272C>T |
| AA Mutation | p.Ala91Val(p.A91V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380607 |
| Start | 17793480:17793480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.842G>A |
| AA Mutation | p.Gly281Asp(p.G281D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380607 |
| Start | 17795590:17795590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.906A>T |
| AA Mutation | p.Glu302Asp(p.E302D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380607 |
| Start | 17789405:17789405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.479A>C |
| AA Mutation | p.Lys160Thr(p.K160T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380607 |
| Start | 17795626:17795626(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146755876 |
| CDS Mutation | c.942C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380607 |
| Start | 17795581:17795581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143422821 |
| CDS Mutation | c.897C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380607 |
| Start | 17791296:17791296(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.690C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |