Primary Site >> Stomach Cancer
Gene >> CADM4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222374 |
| Start | 43627246:43627246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.284G>A |
| AA Mutation | p.Arg95His(p.R95H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222374 |
| Start | 43624231:43624231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.940G>C |
| AA Mutation | p.Val314Leu(p.V314L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222374 |
| Start | 43626804:43626804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.479G>A |
| AA Mutation | p.Arg160Gln(p.R160Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222374 |
| Start | 43626220:43626220(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.568C>T |
| AA Mutation | p.Arg190Cys(p.R190C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222374 |
| Start | 43627268:43627268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.262C>T |
| AA Mutation | p.Arg88Trp(p.R88W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000222374 |
| Start | 43627722:43627722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753225057 |
| CDS Mutation | c.133C>T |
| AA Mutation | p.Arg45Cys(p.R45C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222374 |
| Start | 43625214:43625214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.792T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000222374 |
| Start | 43626146:43626146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199809687 |
| CDS Mutation | c.642G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |