Primary Site >> Stomach Cancer
Gene >> GPR160
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355897 |
| Start | 170084487:170084487(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372339784 |
| CDS Mutation | c.515G>A |
| AA Mutation | p.Arg172His(p.R172H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355897 |
| Start | 170083997:170083997(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766696630 |
| CDS Mutation | c.25T>C |
| AA Mutation | p.Cys9Arg(p.C9R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355897 |
| Start | 170084453:170084453(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.481T>C |
| AA Mutation | p.Tyr161His(p.Y161H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355897 |
| Start | 170084333:170084333(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.361T>A |
| AA Mutation | p.Cys121Ser(p.C121S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355897 |
| Start | 170084784:170084784(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.812C>A |
| AA Mutation | p.Ala271Glu(p.A271E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355897 |
| Start | 170084840:170084840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.868A>G |
| AA Mutation | p.Thr290Ala(p.T290A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355897 |
| Start | 170084878:170084878(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.906A>C |
| AA Mutation | p.Lys302Asn(p.K302N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000355897 |
| Start | 170084119:170084119(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.147C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355897 |
| Start | 170084681:170084681(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.715delA |
| AA Mutation | p.Ile239TyrfsTer22(p.I239Yfs*22) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000355897 |
| Start | 170084680:170084681(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs748213865 |
| CDS Mutation | c.715dupA |
| AA Mutation | p.Ile239AsnfsTer28(p.I239Nfs*28) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |