Primary Site >> Stomach Cancer
Gene >> NLN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380985 |
| Start | 65785797:65785797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845A>G |
| AA Mutation | p.Gln282Arg(p.Q282R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380985 |
| Start | 65792474:65792474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1346C>T |
| AA Mutation | p.Ala449Val(p.A449V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380985 |
| Start | 65781339:65781339(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.740A>G |
| AA Mutation | p.His247Arg(p.H247R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380985 |
| Start | 65792485:65792485(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758153412 |
| CDS Mutation | c.1357G>A |
| AA Mutation | p.Gly453Ser(p.G453S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380985 |
| Start | 65788225:65788225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1066A>G |
| AA Mutation | p.Ile356Val(p.I356V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000380985 |
| Start | 65822881:65822881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769012222 |
| CDS Mutation | c.2081C>T |
| AA Mutation | p.Ala694Val(p.A694V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000380985 |
| Start | 65822831:65822831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148323761 |
| CDS Mutation | c.2031C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |