Primary Site >> Stomach Cancer
Gene >> PLIN4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4512036:4512036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201957398 |
| CDS Mutation | c.1882G>A |
| AA Mutation | p.Val628Met(p.V628M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4510457:4510457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369630072 |
| CDS Mutation | c.3461C>T |
| AA Mutation | p.Ala1154Val(p.A1154V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4512327:4512327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755459936 |
| CDS Mutation | c.1591G>A |
| AA Mutation | p.Val531Met(p.V531M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4516636:4516636(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.194A>G |
| AA Mutation | p.Glu65Gly(p.E65G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4510922:4510922(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776343289 |
| CDS Mutation | c.2996A>C |
| AA Mutation | p.Gln999Pro(p.Q999P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4510517:4510517(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199694958 |
| CDS Mutation | c.3401G>A |
| AA Mutation | p.Arg1134His(p.R1134H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4504754:4504754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3779G>A |
| AA Mutation | p.Cys1260Tyr(p.C1260Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4512537:4512537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376264671 |
| CDS Mutation | c.1381G>A |
| AA Mutation | p.Gly461Ser(p.G461S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4508862:4508862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200494246 |
| CDS Mutation | c.3566G>A |
| AA Mutation | p.Arg1189His(p.R1189H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4513461:4513461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200264250 |
| CDS Mutation | c.457G>A |
| AA Mutation | p.Gly153Ser(p.G153S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4510943:4510943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2975G>T |
| AA Mutation | p.Ser992Ile(p.S992I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4511634:4511634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs75876308 |
| CDS Mutation | c.2284T>G |
| AA Mutation | p.Leu762Val(p.L762V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000301286 |
| Start | 4512710:4512710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755500421 |
| CDS Mutation | c.1208C>T |
| AA Mutation | p.Ala403Val(p.A403V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301286 |
| Start | 4512031:4512031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs549876172 |
| CDS Mutation | c.1887C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301286 |
| Start | 4511746:4511746(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376523137 |
| CDS Mutation | c.2172C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000301286 |
| Start | 4504687:4504687(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752107866 |
| CDS Mutation | c.3846C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |