Primary Site >> Stomach Cancer
Gene >> CD1A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289429 |
| Start | 158256896:158256896(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200592984 |
| CDS Mutation | c.715C>T |
| AA Mutation | p.Arg239Trp(p.R239W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289429 |
| Start | 158256161:158256161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.483C>A |
| AA Mutation | p.Phe161Leu(p.F161L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289429 |
| Start | 158257052:158257052(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779636773 |
| CDS Mutation | c.871G>A |
| AA Mutation | p.Val291Ile(p.V291I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289429 |
| Start | 158256211:158256211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.533T>C |
| AA Mutation | p.Leu178Pro(p.L178P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289429 |
| Start | 158255248:158255248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.223T>G |
| AA Mutation | p.Phe75Val(p.F75V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289429 |
| Start | 158257441:158257441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.904T>G |
| AA Mutation | p.Phe302Val(p.F302V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289429 |
| Start | 158256226:158256226(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.548G>A |
| AA Mutation | p.Cys183Tyr(p.C183Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289429 |
| Start | 158256999:158256999(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.818C>T |
| AA Mutation | p.Ala273Val(p.A273V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000289429 |
| Start | 158255340:158255340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11800924 |
| CDS Mutation | c.315G>T |
| AA Mutation | p.Leu105Phe(p.L105F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |