Primary Site >> Stomach Cancer
Gene >> NRG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361474 |
| Start | 140042692:140042692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.378G>T |
| AA Mutation | p.Lys126Asn(p.K126N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361474 |
| Start | 139848608:139848608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1862C>T |
| AA Mutation | p.Thr621Met(p.T621M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361474 |
| Start | 139871805:139871805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs545628035 |
| CDS Mutation | c.1028G>A |
| AA Mutation | p.Arg343Gln(p.R343Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361474 |
| Start | 139851671:139851671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1705C>T |
| AA Mutation | p.Arg569Cys(p.R569C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361474 |
| Start | 139851664:139851664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1712C>T |
| AA Mutation | p.Ala571Val(p.A571V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361474 |
| Start | 139871815:139871815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1018G>A |
| AA Mutation | p.Gly340Arg(p.G340R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361474 |
| Start | 139855751:139855751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1217T>C |
| AA Mutation | p.Val406Ala(p.V406A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361474 |
| Start | 139853019:139853019(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1301G>A |
| AA Mutation | p.Arg434Gln(p.R434Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361474 |
| Start | 139880873:139880873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770568558 |
| CDS Mutation | c.974G>A |
| AA Mutation | p.Arg325Gln(p.R325Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361474 |
| Start | 139880884:139880884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757530335 |
| CDS Mutation | c.963C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361474 |
| Start | 139851771:139851771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1605G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361474 |
| Start | 139851639:139851639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774248628 |
| CDS Mutation | c.1737C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361474 |
| Start | 139848574:139848574(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1896G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361474 |
| Start | 139851624:139851624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780957553 |
| CDS Mutation | c.1752C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |