Primary Site >> Stomach Cancer
Gene >> PTK7
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230419 |
| Start | 43146684:43146684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2707A>C |
| AA Mutation | p.Ser903Arg(p.S903R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230419 |
| Start | 43145370:43145370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2578C>T |
| AA Mutation | p.Arg860Trp(p.R860W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230419 |
| Start | 43130535:43130535(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.686T>C |
| AA Mutation | p.Leu229Pro(p.L229P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230419 |
| Start | 43130397:43130397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.638A>G |
| AA Mutation | p.Gln213Arg(p.Q213R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230419 |
| Start | 43142072:43142072(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1910T>C |
| AA Mutation | p.Leu637Pro(p.L637P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000230419 |
| Start | 43143536:43143536(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2167A>G |
| AA Mutation | p.Met723Val(p.M723V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230419 |
| Start | 43130551:43130551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.702G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230419 |
| Start | 43142277:43142277(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756545753 |
| CDS Mutation | c.2025G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000230419 |
| Start | 43129011:43129011(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs151242533 |
| CDS Mutation | c.114G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000230419 |
| Start | 43130304:43130325(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.548_569delGGAACCTGACGCTCCGGCCAGC |
| AA Mutation | p.Arg183LeufsTer28(p.R183Lfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000230419 |
| Start | 43146678:43146678(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2704delC |
| AA Mutation | p.Leu902SerfsTer13(p.L902Sfs*13) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |