Primary Site >> Stomach Cancer
Gene >> PLXDC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315392 |
| Start | 39108138:39108138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757179772 |
| CDS Mutation | c.577G>A |
| AA Mutation | p.Val193Ile(p.V193I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315392 |
| Start | 39079144:39079144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143709538 |
| CDS Mutation | c.1010G>A |
| AA Mutation | p.Arg337His(p.R337H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315392 |
| Start | 39087633:39087633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.881C>T |
| AA Mutation | p.Ser294Leu(p.S294L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315392 |
| Start | 39108215:39108215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.500G>T |
| AA Mutation | p.Arg167Leu(p.R167L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315392 |
| Start | 39069893:39069893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1346G>A |
| AA Mutation | p.Gly449Asp(p.G449D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315392 |
| Start | 39079145:39079145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370370043 |
| CDS Mutation | c.1009C>T |
| AA Mutation | p.Arg337Cys(p.R337C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315392 |
| Start | 39108155:39108155(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.560C>T |
| AA Mutation | p.Ser187Phe(p.S187F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000315392 |
| Start | 39087669:39087669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845G>A |
| AA Mutation | p.Arg282His(p.R282H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315392 |
| Start | 39077947:39077947(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1152C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000315392 |
| Start | 39069871:39069871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61742536 |
| CDS Mutation | c.1368G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |