Primary Site >> Stomach Cancer
Gene >> DKK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373970 |
| Start | 52314639:52314639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.205C>T |
| AA Mutation | p.Pro69Ser(p.P69S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373970 |
| Start | 52315047:52315047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.368G>A |
| AA Mutation | p.Arg123His(p.R123H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373970 |
| Start | 52315046:52315046(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138015066 |
| CDS Mutation | c.367C>T |
| AA Mutation | p.Arg123Cys(p.R123C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373970 |
| Start | 52314519:52314519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.85G>T |
| AA Mutation | p.Val29Leu(p.V29L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373970 |
| Start | 52315028:52315028(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.349C>T |
| AA Mutation | p.Arg117Cys(p.R117C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373970 |
| Start | 52316765:52316765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.759A>T |
| AA Mutation | p.Gln253His(p.Q253H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373970 |
| Start | 52314664:52314664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758193742 |
| CDS Mutation | c.230T>C |
| AA Mutation | p.Ile77Thr(p.I77T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373970 |
| Start | 52316558:52316558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.552A>C |
| AA Mutation | p.Gln184His(p.Q184H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000373970 |
| Start | 52314999:52314999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.320G>A |
| AA Mutation | p.Gly107Asp(p.G107D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373970 |
| Start | 52314934:52314934(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.255C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000373970 |
| Start | 52314623:52314623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.189G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | start_lost |
| Transcription ID | ENST00000373970 |
| Start | 52314437:52314437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199874560 |
| CDS Mutation | c.3G>T |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Translation_Start_Site |
| Feature Type | Transcript |