Primary Site >> Esophagus Cancer
Gene >> NES
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156671894:156671894(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2294G>A |
| AA Mutation | p.Arg765Gln(p.R765Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156677074:156677074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.191G>A |
| AA Mutation | p.Arg64Gln(p.R64Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156671261:156671261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2927A>C |
| AA Mutation | p.Asp976Ala(p.D976A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156672212:156672212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs555493675 |
| CDS Mutation | c.1976C>A |
| AA Mutation | p.Ser659Tyr(p.S659Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156676552:156676552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.713G>A |
| AA Mutation | p.Arg238His(p.R238H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156677063:156677063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.202G>A |
| AA Mutation | p.Asp68Asn(p.D68N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000368223 |
| Start | 156670302:156670302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3886C>A |
| AA Mutation | p.Pro1296Thr(p.P1296T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000368223 |
| Start | 156670951:156670951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3237C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000368223 |
| Start | 156669966:156669979(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4209_4222delGGATCGAGATGGGG |
| AA Mutation | p.Trp1403Ter(p.W1403*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |