Primary Site >> Stomach Cancer
Gene >> PDLIM3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284770 |
| Start | 185502356:185502356(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373408599 |
| CDS Mutation | c.1033G>A |
| AA Mutation | p.Ala345Thr(p.A345T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284770 |
| Start | 185523387:185523387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.305A>G |
| AA Mutation | p.Lys102Arg(p.K102R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284770 |
| Start | 185514309:185514309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.359A>G |
| AA Mutation | p.Asn120Ser(p.N120S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000284770 |
| Start | 185525023:185525023(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.242A>G |
| AA Mutation | p.Asp81Gly(p.D81G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284770 |
| Start | 185502435:185502435(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757507673 |
| CDS Mutation | c.954C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000284770 |
| Start | 185502357:185502357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200734614 |
| CDS Mutation | c.1032C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000284770 |
| Start | 185514277:185514277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.391C>T |
| AA Mutation | p.Arg131Ter(p.R131*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |