Primary Site >> Stomach Cancer
Gene >> CD163
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7498980:7498980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.666G>C |
| AA Mutation | p.Trp222Cys(p.W222C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7495360:7495360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201732077 |
| CDS Mutation | c.1141C>T |
| AA Mutation | p.Arg381Cys(p.R381C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7487879:7487879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1629A>C |
| AA Mutation | p.Glu543Asp(p.E543D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7485225:7485225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150182030 |
| CDS Mutation | c.2650A>G |
| AA Mutation | p.Met884Val(p.M884V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7498882:7498882(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.764G>T |
| AA Mutation | p.Gly255Val(p.G255V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7487989:7487989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1519T>C |
| AA Mutation | p.Phe507Leu(p.F507L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7501150:7501150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.446T>C |
| AA Mutation | p.Val149Ala(p.V149A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7496858:7496858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1054A>G |
| AA Mutation | p.Lys352Glu(p.K352E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7496881:7496881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1031A>G |
| AA Mutation | p.Gln344Arg(p.Q344R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7495380:7495380(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1121G>A |
| AA Mutation | p.Arg374Lys(p.R374K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7495359:7495359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780185045 |
| CDS Mutation | c.1142G>A |
| AA Mutation | p.Arg381His(p.R381H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000359156 |
| Start | 7488010:7488010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1498G>A |
| AA Mutation | p.Gly500Ser(p.G500S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359156 |
| Start | 7497033:7497033(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763284228 |
| CDS Mutation | c.879C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359156 |
| Start | 7498941:7498941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.705C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359156 |
| Start | 7487906:7487906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1602A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000359156 |
| Start | 7496976:7496976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749090106 |
| CDS Mutation | c.936C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359156 |
| Start | 7479925:7479925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3415G>T |
| AA Mutation | p.Gly1139Ter(p.G1139*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000359156 |
| Start | 7496960:7496960(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201805567 |
| CDS Mutation | c.952C>T |
| AA Mutation | p.Arg318Ter(p.R318*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |