Primary Site >> Esophagus Cancer
Gene >> NRG1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405005 |
| Start | 32548779:32548779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.53G>A |
| AA Mutation | p.Arg18Gln(p.R18Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405005 |
| Start | 32605571:32605571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764015527 |
| CDS Mutation | c.288A>C |
| AA Mutation | p.Glu96Asp(p.E96D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405005 |
| Start | 32763995:32763995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376858256 |
| CDS Mutation | c.1516G>A |
| AA Mutation | p.Ala506Thr(p.A506T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405005 |
| Start | 32759337:32759337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.962A>G |
| AA Mutation | p.Glu321Gly(p.E321G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405005 |
| Start | 32605582:32605582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.299A>T |
| AA Mutation | p.Asn100Ile(p.N100I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000405005 |
| Start | 32605582:32605582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.299A>C |
| AA Mutation | p.Asn100Thr(p.N100T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405005 |
| Start | 32763829:32763829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752389906 |
| CDS Mutation | c.1350G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000405005 |
| Start | 32760365:32760365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1227A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |