Primary Site >> Stomach Cancer
Gene >> DCBLD2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326840 |
| Start | 98849594:98849594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.438A>C |
| AA Mutation | p.Lys146Asn(p.K146N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326840 |
| Start | 98881607:98881607(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.366T>A |
| AA Mutation | p.Asp122Glu(p.D122E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326840 |
| Start | 98799557:98799557(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2143T>C |
| AA Mutation | p.Tyr715His(p.Y715H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326840 |
| Start | 98822250:98822250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.808G>A |
| AA Mutation | p.Ala270Thr(p.A270T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326840 |
| Start | 98822274:98822274(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200083024 |
| CDS Mutation | c.784A>G |
| AA Mutation | p.Ile262Val(p.I262V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326840 |
| Start | 98881639:98881639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.334C>A |
| AA Mutation | p.Arg112Ser(p.R112S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326840 |
| Start | 98817877:98817877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1104A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326840 |
| Start | 98849474:98849474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.558T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326840 |
| Start | 98819380:98819380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761152287 |
| CDS Mutation | c.909C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000326840 |
| Start | 98819298:98819299(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.990dupA |
| AA Mutation | p.Ala331SerfsTer16(p.A331Sfs*16) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000326840 |
| Start | 98819283:98819284(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1005dupA |
| AA Mutation | p.Pro336ThrfsTer11(p.P336Tfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |