Primary Site >> Stomach Cancer
Gene >> PDPN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621990 |
| Start | 13610474:13610474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.289C>T |
| AA Mutation | p.Pro97Ser(p.P97S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621990 |
| Start | 13614309:13614309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756016330 |
| CDS Mutation | c.380C>T |
| AA Mutation | p.Ser127Leu(p.S127L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621990 |
| Start | 13610460:13610460(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs189019995 |
| CDS Mutation | c.275C>T |
| AA Mutation | p.Ala92Val(p.A92V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621990 |
| Start | 13584074:13584074(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.41C>T |
| AA Mutation | p.Ala14Val(p.A14V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000621990 |
| Start | 13614377:13614377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377220172 |
| CDS Mutation | c.448G>A |
| AA Mutation | p.Val150Ile(p.V150I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621990 |
| Start | 13584078:13584078(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.45G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621990 |
| Start | 13584072:13584072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.39C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000621990 |
| Start | 13607225:13607225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759482997 |
| CDS Mutation | c.120C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000621990 |
| Start | 13614389:13614389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370056113 |
| CDS Mutation | c.460C>T |
| AA Mutation | p.Arg154Ter(p.R154*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000621990 |
| Start | 13614412:13614412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.482+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |