Primary Site >> Stomach Cancer
Gene >> CD177
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618265 |
| Start | 43355738:43355738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.457A>G |
| AA Mutation | p.Lys153Glu(p.K153E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618265 |
| Start | 43361224:43361224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.842C>T |
| AA Mutation | p.Ala281Val(p.A281V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618265 |
| Start | 43362195:43362195(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550497658 |
| CDS Mutation | c.1189G>A |
| AA Mutation | p.Asp397Asn(p.D397N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000618265 |
| Start | 43361465:43361465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200332346 |
| CDS Mutation | c.967C>T |
| AA Mutation | p.Arg323Trp(p.R323W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000618265 |
| Start | 43360344:43360344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs115729962 |
| CDS Mutation | c.699G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000618265 |
| Start | 43362182:43362182(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199770370 |
| CDS Mutation | c.1176G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000618265 |
| Start | 43362167:43362167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760013413 |
| CDS Mutation | c.1161C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000618265 |
| Start | 43362259:43362259(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1258delG |
| AA Mutation | p.Val420TrpfsTer30(p.V420Wfs*30) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |