Primary Site >> Stomach Cancer
Gene >> CENPH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283006 |
| Start | 69191840:69191840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.180G>A |
| AA Mutation | p.Met60Ile(p.M60I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283006 |
| Start | 69191805:69191805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.145C>G |
| AA Mutation | p.Gln49Glu(p.Q49E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000283006 |
| Start | 69194695:69194695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757957352 |
| CDS Mutation | c.239C>T |
| AA Mutation | p.Ala80Val(p.A80V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000283006 |
| Start | 69197075:69197075(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.344delA |
| AA Mutation | p.Asn115ThrfsTer16(p.N115Tfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000283006 |
| Start | 69195770:69195771(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.299dupA |
| AA Mutation | p.Leu101AlafsTer13(p.L101Afs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | splice_donor_variant |
| Transcription ID | ENST00000283006 |
| Start | 69202971:69202971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs541394077 |
| CDS Mutation | c.487+1G>A |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |