Primary Site >> Liver Cancer
Gene >> PDZD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31983634:31983634(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.956A>T |
| AA Mutation | p.Gln319Leu(p.Q319L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32000143:32000143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1126G>C |
| AA Mutation | p.Gly376Arg(p.G376R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32074318:32074318(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3212G>T |
| AA Mutation | p.Gly1071Val(p.G1071V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 31799493:31799493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.245C>G |
| AA Mutation | p.Thr82Ser(p.T82S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32089437:32089437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5989A>T |
| AA Mutation | p.Met1997Leu(p.M1997L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438447 |
| Start | 32074359:32074359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761987954 |
| CDS Mutation | c.3253C>T |
| AA Mutation | p.Pro1085Ser(p.P1085S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 31983170:31983170(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.492G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438447 |
| Start | 32087255:32087255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3807A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000438447 |
| Start | 32088651:32088651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5203G>T |
| AA Mutation | p.Glu1735Ter(p.E1735*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |