Primary Site >> Esophagus Cancer
Gene >> SALL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000614342 |
| Start | 21525467:21525467(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.261T>A |
| AA Mutation | p.Asn87Lys(p.N87K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000614342 |
| Start | 21524847:21524847(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753189477 |
| CDS Mutation | c.881G>A |
| AA Mutation | p.Arg294Gln(p.R294Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000614342 |
| Start | 21523542:21523542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2186G>T |
| AA Mutation | p.Gly729Val(p.G729V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000614342 |
| Start | 21525470:21525486(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.242_258delCCCGGCCTGAGGGTCAC |
| AA Mutation | p.Pro81GlnfsTer2(p.P81Qfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |