Primary Site >> Stomach Cancer
Gene >> PNPLA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336615 |
| Start | 823582:823582(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.752G>A |
| AA Mutation | p.Arg251Gln(p.R251Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336615 |
| Start | 824058:824058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.980C>A |
| AA Mutation | p.Pro327His(p.P327H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336615 |
| Start | 823534:823534(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.704G>A |
| AA Mutation | p.Arg235Gln(p.R235Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336615 |
| Start | 824531:824531(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1184A>T |
| AA Mutation | p.Glu395Val(p.E395V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336615 |
| Start | 821985:821985(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745927123 |
| CDS Mutation | c.448G>A |
| AA Mutation | p.Val150Met(p.V150M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336615 |
| Start | 822474:822474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149864883 |
| CDS Mutation | c.564G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |