Primary Site >> Stomach Cancer
Gene >> PTK6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000542869 |
| Start | 63532607:63532607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.751T>C |
| AA Mutation | p.Tyr251His(p.Y251H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000542869 |
| Start | 63534989:63534989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150179834 |
| CDS Mutation | c.301G>A |
| AA Mutation | p.Ala101Thr(p.A101T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000542869 |
| Start | 63534278:63534278(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.390G>C |
| AA Mutation | p.Trp130Cys(p.W130C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000542869 |
| Start | 63532645:63532645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.713C>A |
| AA Mutation | p.Ala238Asp(p.A238D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000542869 |
| Start | 63534161:63534161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.507C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000542869 |
| Start | 63533603:63533603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61736391 |
| CDS Mutation | c.618C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000542869 |
| Start | 63530791:63530791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761164304 |
| CDS Mutation | c.969C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000542869 |
| Start | 63530085:63530086(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1160_1161delCC |
| AA Mutation | p.Pro387LeufsTer8(p.P387Lfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000542869 |
| Start | 63532585:63532586(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.772dupG |
| AA Mutation | p.Asp258GlyfsTer23(p.D258Gfs*23) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |