Primary Site >> Stomach Cancer
Gene >> PTBP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349038 |
| Start | 805125:805125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770262479 |
| CDS Mutation | c.830G>A |
| AA Mutation | p.Arg277His(p.R277H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349038 |
| Start | 804376:804376(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.373C>T |
| AA Mutation | p.Pro125Ser(p.P125S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349038 |
| Start | 799436:799436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.32G>C |
| AA Mutation | p.Gly11Ala(p.G11A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349038 |
| Start | 808643:808643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1266G>T |
| AA Mutation | p.Glu422Asp(p.E422D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349038 |
| Start | 804617:804617(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.521G>T |
| AA Mutation | p.Gly174Val(p.G174V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349038 |
| Start | 808741:808741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1364C>T |
| AA Mutation | p.Thr455Met(p.T455M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349038 |
| Start | 805056:805056(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775749591 |
| CDS Mutation | c.761G>A |
| AA Mutation | p.Arg254His(p.R254H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349038 |
| Start | 808629:808629(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766285321 |
| CDS Mutation | c.1252C>T |
| AA Mutation | p.Arg418Cys(p.R418C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349038 |
| Start | 804843:804843(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147803014 |
| CDS Mutation | c.621C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349038 |
| Start | 805052:805052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.757C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |