Primary Site >> Stomach Cancer
Gene >> PALB2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261584 |
| Start | 23626343:23626343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766315705 |
| CDS Mutation | c.2641G>A |
| AA Mutation | p.Gly881Ser(p.G881S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261584 |
| Start | 23630110:23630110(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2044T>C |
| AA Mutation | p.Ser682Pro(p.S682P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261584 |
| Start | 23603526:23603526(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773829275 |
| CDS Mutation | c.3494C>T |
| AA Mutation | p.Ser1165Leu(p.S1165L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261584 |
| Start | 23629957:23629957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2197A>G |
| AA Mutation | p.Thr733Ala(p.T733A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261584 |
| Start | 23626269:23626269(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2715G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261584 |
| Start | 23635937:23635937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.609A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261584 |
| Start | 23630024:23630024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774049060 |
| CDS Mutation | c.2130G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261584 |
| Start | 23629949:23629949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs515726082 |
| CDS Mutation | c.2205A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261584 |
| Start | 23621439:23621439(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3036T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261584 |
| Start | 23635707:23635707(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.839delA |
| AA Mutation | p.Asn280ThrfsTer8(p.N280Tfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261584 |
| Start | 23621449:23621449(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs180177131 |
| CDS Mutation | c.3026delC |
| AA Mutation | p.Pro1009LeufsTer6(p.P1009Lfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261584 |
| Start | 23635660:23635660(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs587776408 |
| CDS Mutation | c.886delA |
| AA Mutation | p.Met296Ter(p.M296*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261584 |
| Start | 23603600:23603600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3420G>A |
| AA Mutation | p.Trp1140Ter(p.W1140*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261584 |
| Start | 23629212:23629212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2578G>T |
| AA Mutation | p.Glu860Ter(p.E860*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |