Primary Site >> Stomach Cancer
Gene >> APPL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288266 |
| Start | 57259972:57259972(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1611C>G |
| AA Mutation | p.Ile537Met(p.I537M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288266 |
| Start | 57235610:57235610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.99T>G |
| AA Mutation | p.Ile33Met(p.I33M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288266 |
| Start | 57249512:57249512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764670150 |
| CDS Mutation | c.1016G>A |
| AA Mutation | p.Arg339Gln(p.R339Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288266 |
| Start | 57249436:57249436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.940C>T |
| AA Mutation | p.Arg314Cys(p.R314C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288266 |
| Start | 57260692:57260692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1760T>C |
| AA Mutation | p.Val587Ala(p.V587A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000288266 |
| Start | 57259938:57259938(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs551759110 |
| CDS Mutation | c.1577G>A |
| AA Mutation | p.Arg526His(p.R526H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288266 |
| Start | 57268466:57268466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1962T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288266 |
| Start | 57240524:57240524(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.345T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288266 |
| Start | 57249408:57249408(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201817839 |
| CDS Mutation | c.912G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000288266 |
| Start | 57269606:57269606(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2049G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000288266 |
| Start | 57242893:57242893(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs749401724 |
| CDS Mutation | c.460delA |
| AA Mutation | p.Arg154GlufsTer6(p.R154Efs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000288266 |
| Start | 57260680:57260680(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1752delT |
| AA Mutation | p.Phe584LeufsTer42(p.F584Lfs*42) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000288266 |
| Start | 57237544:57237544(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.210delA |
| AA Mutation | p.Lys70AsnfsTer13(p.K70Nfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000288266 |
| Start | 57242892:57242893(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs757369141 |
| CDS Mutation | c.460dupA |
| AA Mutation | p.Arg154LysfsTer4(p.R154Kfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |